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Post-Polio Syndrome: Impact of Humoral Immune Deficiencies, Poliovirus Neutralizing Antibodies, Vitamin D Deficiency

A peer-reviewed version of this preprint was published in:
Vaccines 2025, 13(9), 939. https://doi.org/10.3390/vaccines13090939

Submitted:

22 July 2025

Posted:

23 July 2025

Read the latest preprint version here

Abstract
Background/Objectives: This study investigated susceptibility factors that may contribute to Post-Polio Syndrome (PPS) in elderly polio survivors. Methods: Serum immunoglobulin (Ig) levels, poliovirus neutralizing antibodies (PV NAb), and vitamin D status were evaluated in 80 PPS patients, 40 family members, and 89 healthy controls. Results: A significant number of PPS patients and their family members showed reduced levels of total IgG and/or IgA, and specific IgG subclasses indicating a high prevalence of primary humoral immunodeficiencies within these groups. Despite these Ig deficits, PV NAb titers were similar across all groups, indicating high protection against poliovirus, likely due to vaccination campaigns with live virus in Italy and intense exposure to poliovirus especially in long-term rehabilitation institutions. However, a small group of PPS subjects lacked neutralizing antibodies for specific poliovirus serotypes, suggesting more severe antibody deficiencies. Additionally, PPS subjects had a high prevalence of vitamin D deficiency, which likely increases their risk for osteoporosis/osteopenia and fractures. It's unclear if this deficiency was present also in their infancy, potentially enhancing their susceptibility to poliovirus. Conclusions: Overall, the findings indicate that genetic, immunological, or nutritional factors may increase individual susceptibility to the pathogenic effects of poliovirus. This study - limited to serum antibodies - highlights the complex relationship between immune status and long-term health in aging polio survivors. The results emphasize the need for potent poliovirus drugs and vaccines to help contain possible outbreaks but also – for poliomyelitis survivors - to avoid or mitigate the progression to PPS, the latest phase of this devastating disease.
Keywords: 
post-polio syndrome
;  
poliovirus
;  
virus susceptibility
;  
antibody deficiency
;  
neutralizing antibodies
;  
vitamin D
;  
polio vaccine
Subject: 
Medicine and Pharmacology  -   Epidemiology and Infectious Diseases

1. Introduction

Polioviruses (PVs) belong to the C species of the Enterovirus (EV) genus and comprise three types (1 to 3). During the pre-vaccine era, approximately 1 in 190 infections with PV type 1 resulted in paralytic poliomyelitis (PPM), a substantially higher incidence compared to PV-2 or PV-3 infections, which led to PPM in only 1 in 1,100 to 1,900 individuals [1]. Despite the understanding of infectivity-to-paralysis ratios, the precise mechanisms governing susceptibility to PV infections and the development of PPM remain unclear. Research has explored various predisposing factors, including host genetic and immunological elements, alongside variables such as age at infection, hygienic conditions, lactation practices, and nutritional status.
Susceptibility to infectious agents is influenced by the host’s genetic background [2]. Accordingly, studies have suggested that specific genetic factors may modulate the outcome of enteroviral diseases. Specifically, HLA haplotypes could contribute to PPM resistance [3] and rare mutations in the PV receptor CD155 may favor the development of PPM [4]. In addition, single nucleotide polymorphisms (SNPs) in TLR3 and TLR7 may confer susceptibility to severe forms of EV-induced hand, foot, and mouth disease (HFMD) [2] and variants of the EV-A71 receptor PSGL-1 may predispose to severe HFMD. Despite these findings, no single genetic factor is believed to solely regulate susceptibility to PVs.
Immunologically, inborn errors of immunity (IEIs) are associated with enhanced susceptibility to infections [5] and, particularly, to EV infections [6]. Chronic shedding of vaccine-derived poliovirus (VDPV) occurs in individuals with defects in B-cell-mediated immunity. Most VDPV carriers present with a Predominantly Antibody Deficiency (PAD), but approximately one fifth are diagnosed with a combined immunodeficiency [7]. Crucially, neutralizing secretory IgA plays a prominent role in limiting PV replication in mucosae of the digestive tract, while neutralizing IgG protects the central nervous system (CNS) from PV entry.
Long experience from polio vaccine campaigns underscores the need for implementation of comprehensive public health strategies that address malnutrition, limited access to clean water and inadequate sanitation. All these elements promote morbidity, mortality, and the transmission of viruses. The concurrent administration of vitamin A supplements has enhanced the efficacy of some polio vaccine campaigns [8,9]. Preclinical research in mice shows that co-administration of inactivated PV vaccine with vitamin D3 (cholecalciferol) enhances the systemic and mucosal antiviral immune responses [10]. Determined by diet and sunlight exposure (as well as by genetic background), an individual’s vitamin D status is best evaluated by measuring serum levels of 25-hydroxyvitamin D [11].
Vitamin D plays key roles in immunomodulation and bone health. Recently, it has been demonstrated that vitamin D deficiency/insufficiency was present in the majority of patients hospitalized with COVID-19 or influenza A, that low levels correlate with disease severity and tend to persist indefinitely in survivors [12].
In humans, vitamin D supplementation modulates the immune transcriptome upregulating the presentation of antigens and viral response pathways. However, some immune signaling pathways are downregulated, including tumor necrosis factor-alpha and interleukin (IL)-17 [13] as well as the production in vitro of IL-2 and IFN-gamma [14]. It was also shown that vitamin D promotes the transition from pro-inflammatory IFN-gamma Th1 cells to suppressive IL-10+ cells [15].
Recent clinical trials demonstrated a protective activity of vitamin D against the progression of Multiple Sclerosis (MS) [16,17], an immuno-mediated disease of possible viral origin [18]. Thus, investigating the vitamin D status in people suffering severe infections may be of clinical relevance.
To advance the understanding of the individual susceptibility to paralytic poliomyelitis and to its long-term sequelae, we investigated aging polio survivors diagnosed with the Post-Polio Syndrome (PPS), a disorder coded as G14 in the International Classification of Diseases (ICD-10-CM) with the aim to assess potential immunoglobulin (Ig) deficiencies, poliovirus-neutralizing antibody (PV NAb) titers, and vitamin D levels.

2. Materials and Methods

2.1. Ethics

The study was approved by the Ospedale di Circolo & Fondazione Macchi Research Ethics Committee – Varese, Italy [REC: 0018898/2011; 0041619/2012; 003645/2013; 00811/2018] and the Policlinico GB Rossi, Research Ethics Committee – Verona, Italy [Multicenter study NCT02176863/2014-2022]. Studies have been performed in accordance with the Declaration of Helsinki and its revisions. Before clinical assessment, all patients and controls provided informed written consent to medical procedures and studies of their biological samples.

2.2. Participating Hospitals, PPS Patients and Control Groups

A total of 209 individuals were investigated. Participants to the study were recruited between February 2011 and November 2019 at tertiary care Hospitals of Northern Italy specializing in Neurology and Rehabilitation: Policlinico GB Rossi, Verona, Italy; Villa Beretta Rehabilitation Center, Costa Masnaga, Italy; Ospedale di Circolo e Fondazione Macchi, Varese, Italy. Polio survivors had a verified diagnosis of poliomyelitis, supportive clinical data, imaging data, and electromyographic findings. Exclusion criteria: history of cerebrovascular disease, neuropathy from causes other than polio, congenital or acquired immune deficiencies, diabetes mellitus, drug or alcohol dependence. Blood samples were drawn in BD Vacutainer serum tubes after overnight fasting, either at the Ospedale di Circolo e Fondazione Macchi in Varese or procured at participating hospitals and shipped in dry ice to the laboratory in Varese. Samples were centrifuged at 4°C, supernatants were divided into aliquots and stored without delay at -80°C. Subjects of Control Groups consenting to take part in the study were evaluated at the Ospedale di Circolo e Fondazione Macchi in Varese. Table 1 summarizes the demographic and clinical data of the subjects investigated. Although the groups were not deliberately matched, their age, biological sex and socioeconomic status were suitable for comparison.
Polio survivors were admitted to participating Hospitals because of progressive worsening of weakness and fatigue during daily and/or working activities. Diagnosis of PPS was based on criteria of the European Federation of Neurological Societies (Farbu et al. 2006). PPS is a slowly progressive condition characterized by new neuromuscular symptoms that occur after several years of clinical stability in people with a prior history of poliomyelitis [19,20]. Clinical features include new muscular weaknesses persisting for at least one year, fasciculations, atrophy of previously unaffected limbs, bulbar-innervated muscles, muscles of respiration, combined with chronic fatigue, joint and muscle pain, cold intolerance, swallowing problems, a depressive syndrome and sleep disorders.
Control groups included: healthy controls (blood donors) and family members of PPS subjects who had lived with them for at least five years (64% were siblings and offspring, 36% were partners or kindred). Blood samples from each PPS subject and his/her family member(s) were obtained on the same day.

2.3. Quantification in Serum of Major Ig Classes and IgG Subclasses

Blood was drawn in BD Vacutainer serum tubes and centrifuged within two hours. Serum samples were stored at -80°C. According to manufacturers’ protocols, Ig of the three major classes were measured using the IgG, IgA, IgM kits of Beckman-Coulter (Cassina de’Pecchi, Italy) in conjunction with the IMMAGE Immunochemistry system and calibrators. Quantification of IgG subclasses was performed using the Peliclass IgG subclass Plus kit (Sanquin, Amsterdam, NL). The assay is based on nephelometry for IgG1 and IgG2 and latex turbidimetry for IgG3 and IgG4. The WHO 67/97 preparation was used as a reference. Calibrators had the following values: 6.210 g/L for IgG1, 3.450 g/L for IgG2, 0.390 g/L for IgG3, 0.591 g/L for IgG4. Regarding Ig levels, a guide to reference ranges for adult Caucasians has been used [21]. By means of the above reported methods, limits for significantly low Ig levels have been validated at our own laboratory (Ospedale di Circolo, Varese, Italy) in a cohort of 120 healthy adult blood donors (median age 51.2 yrs; IQR: 32.5-61.7 yrs). The obtained intervals encompass ≥95% of the values found in the control group of blood donors.

2.4. Poliovirus Neutralization Assays and Biosafety

PV NAb titers in serum were determined at the National Institute for Health and Welfare (THL - Helsinki, Finland). Tests were carried out according to good laboratory and microbiological practices [22] using a standardized microneutralization test for the three PV serotypes [23]. PV-susceptible HeLa cells expressing the CD155/PVR (poliovirus receptor) were cultured in 96-well microplates with 100 ml of Eagle’s essential medium supplemented with 5% FBS and antibiotic mixture. Following complement inactivation (56°C for 30 minutes), serum samples were serially diluted two-fold in cell culture medium (from 1:4 to 1:8192). These dilutions were prepared in 75 µL working volumes, with 8 replicates per dilution. Then, 75ml of medium containing 100 TCID50 of the appropriate PV serotype was added to each well. The virus and serum were thoroughly mixed via vortex. The microplates were incubated at 36°C for 1hr. The content of each well (150 ml) was then transferred to a 96 well microplate containing Hela cell monolayers in 100ml of medium. Microplates were incubated for 6 days at 36°C in air with 5% CO2. The titer of PV NAb represents the highest dilution of serum capable of preventing virus-induced cytopathic effect in 4 out of 8 cell cultures tested in parallel. NAb titers were calculated using the Reed-Muench formula and are the only measurement known to correlate with protection from PV infection. Titers ≥1:8 are considered protective.

2.5. Determination of 25-Hydroxyvitamin D in Serum

Since 25(OH)D has a half-life of about 15-30 days and its levels directly reflect the body’s vitamin D stores from all sources, its levels in serum are a reliable indicator of the vitamin D status [11]. 25(OH)D was quantified by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MSMS). Solvent extraction and protein precipitation of 100 µl of serum were conducted using a commercial assay from PerkinElmer (Milan, Italy) which included calibrators and quality controls. Samples (50 ml) were injected into the HPLC-MSMS system (UHPLC Agilent 1290 Infinity II, Santa Clara, CA and MSMS AB-Sciex API4000, Concord, ON, Canada). Intra- and inter-assay imprecision of the assay were 4.7% and 4.3%, respectively. Sensitivity was 4 nmol/L. According to the Endocrine Society Clinical Practice Guideline on Vitamin D [24], serum 25(OH)D concentrations were interpreted as deficiency (≤50 nmol/L), insufficiency (52.5-72.5 nmol/L), and sufficiency (75-250 nmol/L).

2.6. Statistics

Normal distribution of values was estimated using the D’Agostino & Pearson omnibus normality test. Groups were compared using the Mann-Whitney U test, Fisher’s exact test, Kruskal-Wallis test, Chi-square test with Bonferroni correction (GraphPad Prism, v.10). Results are presented as median with interquartile range (IQR), mean ± SD or ±95% confidence interval (CI), geometric mean ± SD or ±95% confidence interval (CI). Two-sided p<0.05 was considered statistically significant.

3. Results

3.1. Study Groups

Two hundred nine adult participants were recruited from hospitals in the Veneto and Lombardy regions, forming three distinct study groups detailed in Table 1. Although these groups were not deliberately matched, their age, biological sex, and socioeconomic status were found to be comparable.
Among the participants, 80 polio survivors were identified as affected by PPS through comprehensive medical history review, clinical examination, and instrumental diagnostic tests. PPS cases had a median age of 56.0 years (interquartile range [IQR]: 51.8–62.0), with their diagnosis having been established at a median age of 49 years (IQR: 43.0–56.0 years). Given that the onset of Acute Paralytic Polio (APP) occurred at a median age of 2.0 years (IQR: 1.0–3.3 years), PPS typically manifested approximately 47 years after the acute disease.
The vaccination rate among PPS cases was notably low (22.1%), a finding consistent with the fact that most were born in the 1950s (before polio vaccines were widely available) and only a small proportion had been vaccinated following their acute polio episode. In contrast, vaccination rates were significantly higher in the healthy control group (100%) and among family members of PPS cases (57.7%). These divergent vaccination rates are particularly relevant for the subsequent comparison of PV antibody titers across the study groups. It should be noted that, due to limitations in sample availability, not all planned assays were performed for every study participant.

3.2. Immunoglobulin Levels and Deficiencies Across the Study Groups

Serum Ig levels are presented as median ± 95% confidence interval (CI). Figure 1 illustrates the results for the three major Ig classes: IgG, IgA, and IgM. Compared to healthy blood donors, IgG levels were significantly reduced by approximately 16% in both the family member group and among PPS cases. Similarly, IgA levels showed a significant reduction of about 35% in both the family member and PPS groups. In contrast, no significant differences were observed in IgM levels across any of the groups.
Further analysis of IgG subclasses, detailed in Figure 2, revealed a significant reduction in IgG1 levels among PPS cases. Family members, however, exhibited only a minor, non-significant decrease in IgG1. Relative to healthy blood donors, statistically significant reductions were observed for IgG2, IgG3, and IgG4 levels in both the family member and PPS groups.
Given that serum Ig levels were not normally distributed among subjects in the three study groups, the presence of outliers was evident. Further analysis revealed that PPS cases and their family members exhibited higher percentages of Ig levels below the lower cutoff values established from adult reference subjects (blood donors). Table 2 specifically shows that IgA, IgG, IgG1, and IgG3 exhibited the highest frequencies of concentrations below the cutoff (ranging from 10% to 34% of cases).

3.3. Poliovirus-Neutralizing Antibody Titers

PV NAb titers are presented as geometric mean ± 95% CI. Titrations were performed using eight replicates per dilution. As illustrated in Figure 3, nearly all subjects across the three study groups exhibited protective titers against all three PV types. Geometric means ranged from 1:96 to 1:384 across serotypes and groups. The maximum observed titers were 1:12,288 for both PV-1 and PV-2, and 1:3,072 for PV-3.
Significant differences in PV NAb titers across groups were detected only for PV-1. Specifically, family members exhibited lower mean PV-1 titers than blood donors. Conversely, while PPS cases did not significantly differ from blood donors in PV-1 titers, they showed significantly higher titers than subjects in the family member group. For PV-2 and PV-3, NAb titers were not statistically different among groups.
The polio vaccination rate varied considerably among groups, being 100% in blood donors, 55.3% in family members, and 21.3% in PPS cases (Table 3). Consistent with these vaccination rates and other factors, non-protective PV NAb titers (<1:8) were absent in blood donors, rare among family members (2.7%), and slightly more represented among PPS cases (6.7% to 10.7%), as also shown in Table 3.

3.4. Serum 25-Hydroxyvitamin D Levels

Serum 25-hydroxyvitamin D [25(OH)D] concentrations are presented as median ± 95% confidence interval (CI). Measurements were performed using high-performance liquid chromatography-tandem mass spectrometry.
Figure 4 illustrates the 25(OH)D data for the three study groups. While median vitamin D levels did not significantly differ between blood donors and family members of PPS cases (85 nmol/L and 73 nmol/L, respectively), the PPS group’s median value (54 nmol/L) was significantly lower than that of both blood controls (p<0.0001) and their family members (p<0.0036).
Furthermore, as depicted in Figure 5, interpreting 25(OH)D concentrations according to the Endocrine Societies Guidelines [11,24] revealed that PPS cases exhibited the highest prevalence of vitamin D deficiency and insufficiency (46% and 36%, respectively). This was followed by their family members (27% deficiency, 23% insufficiency). As anticipated, healthy blood donors maintained satisfactory serum 25(OH)D levels, with only 8% presenting deficient and 10% insufficient levels.

4. Discussion

Our key findings indicate that a significant proportion of PPS cases exhibit reduced levels of IgG and/or IgA, supported by varying degrees of reduction in specific IgG subclasses. Thus, individuals with paralytic polio and subsequent PPS demonstrate variable types of humoral immunodeficiencies. In addition, PPS cases exhibited PV NAb titers not substantially different from those of controls but had a deficient/insufficient vitamin D status.
Notably, humoral immunodeficiencies were found to a comparable extent in their family members. This observation is particularly challenging to fully explain. While many of the family members investigated were first-degree relatives of PPS cases, approximately one-third lacked a direct genetic connection to the probands.
Evidence is being accumulating that individuals with primary immunodeficiencies are at an increased risks of vaccine-associated paralytic poliomyelitis (VAPP) and prolonged excretion of vaccine-derived PV [25]. Compared to humoral immunodeficiency patients, subjects with combined immunodeficiency show lower rates of VAPP that arises from 2 months to 4 years post-exposure to live polio vaccines [26]. The wide spectrum of Predominant Antibody Deficiencies (PAD) encompasses a group of primary disorders characterized by dysfunctional antibody production leading to low levels of one or more Ig classes. These conditions - as reviewed by Gilchrist and Dolen [27], Griffin and Dolen [28]) and others [29] - may either present with recurrent infections and reduced vaccine responses or be asymptomatic. PAD include Common Variable Immunodeficiency (CVID) which is very rare and characterized by low IgG and IgA levels; X-linked agammaglobulinemia (XLA), also very rare and marked by a near-complete absence of B cells with very low levels of all Ig classes; selective IgA deficiency whose frequency is 1:150 to 1:2000 in Caucasians but very rare in the Japanese; IgG subclass deficiency whose prevalence can be up to 2% of healthy individuals when only considering low levels; other less common defects. All of these, lessen antiviral defenses and facilitate the establishment of chronic infections [25,30].
Overall, the observed reductions of Ig concentration, though of moderate magnitude, were statistically significant and consistently present across six different Ig classes or subclasses. This indicates a clear predisposition to serum antibody deficiencies in both the PPS group and their family members. Notably, the most pronounced deficit occurred for IgA, an antibody class involved in mucosal surface protection, but deficits were also detected for IgG, IgG1 and IgG3. Properties of IgG subclasses classes have been reviewed recently [31].
Regarding susceptibility to PVs, it would be important to assess the IgA1 and IgA2 levels in mucosal secretions of the digestive and respiratory tracts of individuals with acute paralytic poliomyelitis or PPS. This is due to dimeric IgA’s significantly higher virus-neutralizing activity compared to a corresponding IgG antibody, which confers enhanced protection. [32].
IgG1 serves as the principal subclass involved in the immune response to protein antigens; therefore, its deficiency may result in inadequate antibody responses to viral agents. For instance, deficient IgG responses to the nucleocapsid and glycoprotein antigens of the Severe Fever with Thrombocytopenia Syndrome (SFTSV), a Bunyavirus, have been associated with fatal outcomes [33].
IgG3 is a uniquely effective antibody with the potential for triggering effector functions including complement activation, antibody-mediated phagocytosis, antibody-mediated cellular cytotoxicity [34]. During arboviral Chikungunya fever, the host immune response is predominantly characterized by an IgG3 response. Some patients experiencing high viremia rapidly developed robust IgG3 antibody levels. Despite enduring a more severe viremic phase, these individuals cleared the virus more rapidly, did not experience persistent arthralgia, and exhibited long-term protection[35]. Thus, IgG3 antiviral antibodies, despite their strong inflammatory potential, constitute an essential component of antiviral defenses.
Therefore, given the critical importance of antibody responses against enteroviruses, PPS patients might represent individuals whose weak resistance against PVs could be complicated by the subsequent establishment of persistent infection (Toniolo et al., 2025 submitted).
In contrast to the observed Ig deficits in serum, PV NAb titers were substantially similar across the three study groups, an unexpected finding. When planning the study, we hypothesized that PPS cases, given their low polio vaccination prevalence, would primarily exhibit high antibody responses to a single PV serotype, i.e., that causing the acute disease and, potentially, any subsequent persisting infection [36]. Hence, the presence of high NAb titers to heterologous PV serotypes in this group was unanticipated. Actually, fully vaccinated blood donors had the highest mean titers, followed by PPS patients and their family members. However, differences in titers were minimal and statistically significant only about PV-1. It should be noted, however, that a small proportion of PPS subjects lacked neutralizing antibodies, especially PV-2 and PV-3. These rare cases could represent individuals impacted by more severe antibody deficits.
The mean poliovirus neutralizing antibody (PV NAb) titers observed in this study are consistent with previous results obtained in adult populations from Italy [37] and Belgium [38]. This high prevalence and titer of PV antibodies (>95%) in our aged subjects can be attributed to past intensive vaccination campaigns with live virus and – in the early vaccine era – to the frequent exposure to PV carriers.
An additional consideration for interpreting this data, however, is that PPS subjects - and potentially their family members - had experienced prolonged contact with poliomyelitis patients. Specifically, following the onset of APP, in Italy severe polio cases attended specialized Rehabilitation Wards which became active from the 1950s onwards [39]. Within these environments, exposure to either wild-type or Sabin PV strains was frequent and intense.
As a final point, the prevalence of 25(OH)vitamin D deficiency was very high in PPS subjects indicating an inadequate vitamin D status. The deficit was less pronounced in their family members and virtually absent in healthy blood donors. The results were not surprising. Individuals with PPS, though not experiencing malnutrition, are generally less exposed to open air, sunlight and physical exercise because of their clinical condition. In addition, their vitamin status indicates that they were not or inadequately supplemented with vitamin D.
Maintaining adequate vitamin D status is crucial, considering that most vitamin D is synthesized in the skin following UVB exposure, with minimal contribution from typical unfortified diets. Acknowledging the usual seasonal decline in 25(OH)D levels during winter, a target of at least 75 nmol/L is recommended for vitamin D sufficiency [11]. The inadequate vitamin D status in PPS patients is particularly concerning. Due to mobility deficits and aging, individuals with PPS frequently experience falls and often present with osteopenia/osteoporosis [40]. This combination collectively places them at a significantly increased risk for fractures. Therefore, vitamin D supplementation could confer beneficial effects [41].
Beyond its established role in bone health, vitamin D is also crucial for potentiating and regulating antimicrobial defenses [42]. This raises an intriguing, albeit difficult to assess, question: were individuals currently diagnosed with PPS also vitamin D-deficient during infancy when APP manifested? While retrospective assessment is challenging given the currently rare incidence of new polio cases, it is known that vitamin D deficiency remains prevalent (>10%) in pediatric populations worldwide, even though most biochemically deficient children remain asymptomatic [43]. Furthermore, historical data indicate that children in countries with widespread malnutrition and compromised hygienic conditions are at a higher risk of paralytic polio [44], suggesting that complex environmental factors influence polio susceptibility.
This study presents limitations that warrant consideration when interpreting the findings. Firstly, the relatively modest sample size of the study groups may limit the statistical power and generalizability of results. Secondly, despite efforts, perfect matching of cases and controls regarding age and seasonal variations was not feasible, which could have influenced immunological parameters and vitamin D levels. A further methodological limitation was the exclusive focus on serum antibody responses. This precluded the evaluation of secretory IgA (sIgA), a key determinant of mucosal immunity and resistance against PVs.

5. Conclusions

Collectively, the results indicate that, despite the efficacy of current preventive vaccines, certain individuals remain particularly susceptible to the paralytogenic potential of PVs due to genetic, immunological, or nutritional factors. This underscores the urgent need for effective PV antivirals to block possible outbreaks [45,46] but also - for polio survivors – the development of potent drugs and PV vaccines aimed at preventing or retarding the development of PPS, the latest phase of poliomyelitis [47,48].

Author Contributions

Conceived and designed the study: A.T., K.C., S.M., F.M., G.B., G.F. Performed the experiments: G.M., A.G., A.T., K.C., A.N., A.S. Provided samples, diagnosis and interpretation of clinical data: S.M., A.T., F.M., G.B., G.F. Analyzed and interpreted the data: A.T., K.C., G.M., S.M., F.M., G.B., G.F. Wrote the initial draft of the paper: A.T. and S.M. Revised the paper and prepared its final version: A.T., S.M., K.C., F.M., G.B., G.F. All authors have read and agreed to the published version of the manuscript.

Funding

Regione Lombardia (Milano, Italy) grant No. 13465/2013 to AT; Post-Polio Health International (St Louis, MO) grant 2009 to AT and Eighth Award-2014 to AT and KC. Administrative support: Associazione Interregionale Disabili Motori (AIDM), Ospedale di Malcesine (Verona, Italy).

Institutional Review Board Statement

The study was approved by the Ospedale di Circolo & Fondazione Macchi Research Ethics Committee – Varese, Italy [REC: 0018898/2011; 0041619/2012; 003645/2013; 00811/2018] and the Policlinico GB Rossi, Research Ethics Committee – Verona, Italy [NCT02176863 2014-2023]. The procedures employed in the study are in accordance with the ethical standards of the Local Ethics Committees and with the 1964 Helsinki Declaration and its later amendments.

Data Availability Statement

Datasets are available to readers upon reasonable request to the corresponding Authors.

Acknowledgments

Poliovirus neutralizing antibodies have been determined by Dr. Merja Roivainen and her team at the Finnish Institute for Health and Welfare (Helsinki, Finland). Her professional contributions, cooperative efforts, friendly and expert advice are gratefully acknowledged. Special thanks to the polio patients at Villa Beretta Rehabilitation Center who inspired this work. We are indebted to all polio survivors, their family members, and adult blood donors who participated in the study. We express our deep gratitude to Dr. Carlo Lucchina (Regione Lombardia, Milano, Italy) and to the Leaders of Post-Polio Associations which promoted studies on post-polio syndrome: Joan L Headley (PPHI, St Louis, MO); Denis Montagnoli and Roberto Bassi (AIDM, Malcesine, Italy); Nadia Gatti (CONDAV, Sabbioneta, Italy); John R McFarlane (European Polio Union, Huldenberg, Belgium); Mary-ann Liethof (Polio Australia Incorporated, Kew, Victoria, Australia). We thank the Global Virus Network (Tampa, FL) and the Network of Pancreatic Organ Donors, Virus Group (Miami, FL) for encouragement and scientific advice.

Conflicts of Interest

The authors have no relevant financial or non-financial competing interests to disclose. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

References

  1. Nathanson, N.; Kew, O.M. From Emergence to Eradication: The Epidemiology of Poliomyelitis Deconstructed. American Journal of Epidemiology 2010, 172, 1213–1229. [CrossRef]
  2. Tian, C.; Hromatka, B.S.; Kiefer, A.K.; Eriksson, N.; Noble, S.M.; Tung, J.Y.; Hinds, D.A. Genome-Wide Association and HLA Region Fine-Mapping Studies Identify Susceptibility Loci for Multiple Common Infections. Nat Commun 2017, 8, 599. [CrossRef]
  3. Van Eden, W.; Persijn, G.G.; Bijkerk, H.; De Vries, R.R.P.; Schuurman, R.K.B.; Van Rood, J.J. Differential Resistance to Paralytic Poliomyelitis Controlled by Histocompatibility Leukocyte Antigens. Journal of Infectious Diseases 1983, 147, 422–426. [CrossRef]
  4. Kindberg, E.; Ax, C.; Fiore, L.; Svensson, L. Ala67Thr Mutation in the Poliovirus Receptor CD155 Is a Potential Risk Factor for Vaccine and Wild-type Paralytic Poliomyelitis. Journal of Medical Virology 2009, 81, 933–936. [CrossRef]
  5. Bucciol, G.; Moens, L.; Bosch, B.; Bossuyt, X.; Casanova, J.-L.; Puel, A.; Meyts, I. Lessons Learned from the Study of Human Inborn Errors of Innate Immunity. Journal of Allergy and Clinical Immunology 2019, 143, 507–527. [CrossRef]
  6. Riller, Q.; Schmutz, M.; Fourgeaud, J.; Fischer, A.; Neven, B. Protective Role of Antibodies in Enteric Virus Infections: Lessons from Primary and Secondary Immune Deficiencies. Immunological Reviews 2024, 328, 243–264. [CrossRef]
  7. Guo, J.; Bolivar-Wagers, S.; Srinivas, N.; Holubar, M.; Maldonado, Y. Immunodeficiency-Related Vaccine-Derived Poliovirus (iVDPV) Cases: A Systematic Review and Implications for Polio Eradication. Vaccine 2015, 33, 1235–1242. [CrossRef]
  8. Duintjer Tebbens, R.J.; Pallansch, M.A.; Cochi, S.L.; Wassilak, S.G.F.; Linkins, J.; Sutter, R.W.; Aylward, R.B.; Thompson, K.M. Economic Analysis of the Global Polio Eradication Initiative. Vaccine 2010, 29, 334–343. [CrossRef]
  9. Tangermann, R.H.; Costales, M.; Flavier, J. Poliomyelitis Eradication and Its Impact on Primary Health Care in the Philippines. Journal of Infectious Diseases 1997, 175, S272–S276. [CrossRef]
  10. Ivanov, A.P.; Dragunsky, E.M.; Chumakov, K.M. 1,25-Dihydroxyvitamin D3 Enhances Systemic and Mucosal Immune Responses to Inactivated Poliovirus Vaccine in Mice. J INFECT DIS 2006, 193, 598–600. [CrossRef]
  11. Giustina, A.; Bilezikian, J.P.; Adler, R.A.; Banfi, G.; Bikle, D.D.; Binkley, N.C.; Bollerslev, J.; Bouillon, R.; Brandi, M.L.; Casanueva, F.F.; et al. Consensus Statement on Vitamin D Status Assessment and Supplementation: Whys, Whens, and Hows. Endocrine Reviews 2024, 45, 625–654. [CrossRef]
  12. Hurst, E.A.; Mellanby, R.J.; Handel, I.; Griffith, D.M.; Rossi, A.G.; Walsh, T.S.; Shankar-Hari, M.; Dunning, J.; Homer, N.Z.; Denham, S.G.; et al. Vitamin D Insufficiency in COVID-19 and Influenza A, and Critical Illness Survivors: A Cross-Sectional Study. BMJ Open 2021, 11, e055435. [CrossRef]
  13. Yeh, W.Z.; Gresle, M.; Lea, R.; Taylor, B.; Lucas, R.M.; Ponsonby, A.-L.; Mason, D.; Andrew, J.; Campbell, H.; Morahan, J.; et al. The Immune Cell Transcriptome Is Modulated by Vitamin D3 Supplementation in People with a First Demyelinating Event Participating in a Randomized Placebo-Controlled Trial. Clinical Immunology 2024, 262, 110183. [CrossRef]
  14. Saggese, G.; Federico, G.; Balestri, M.; Toniolo, A. Calcitriol Inhibits the PHA-Induced Production of IL-2 and IFN-γ and the Proliferation of Human Peripheral Blood Leukocytes While Enhancing the Surface Expression of HLA Class II Molecules. J Endocrinol Invest 1989, 12, 329–335. [CrossRef]
  15. Chauss, D.; Freiwald, T.; McGregor, R.; Yan, B.; Wang, L.; Nova-Lamperti, E.; Kumar, D.; Zhang, Z.; Teague, H.; West, E.E.; et al. Autocrine Vitamin D Signaling Switches off Pro-Inflammatory Programs of TH1 Cells. Nat Immunol 2022, 23, 62–74. [CrossRef]
  16. Nolan, T. Vitamin D for Multiple Sclerosis … and Other Research. BMJ 2025, r601. [CrossRef]
  17. Thouvenot, E.; Laplaud, D.; Lebrun-Frenay, C.; Derache, N.; Le Page, E.; Maillart, E.; Froment-Tilikete, C.; Castelnovo, G.; Casez, O.; Coustans, M.; et al. High-Dose Vitamin D in Clinically Isolated Syndrome Typical of Multiple Sclerosis: The D-Lay MS Randomized Clinical Trial. JAMA 2025. [CrossRef]
  18. Soldan, S.S.; Lieberman, P.M. Epstein–Barr Virus and Multiple Sclerosis. Nat Rev Microbiol 2023, 21, 51–64. [CrossRef]
  19. Howard, R.S. Poliomyelitis and the Postpolio Syndrome. BMJ 2005, 330, 1314–1318. [CrossRef]
  20. Farbu, E.; Gilhus, N.E.; Barnes, M.P.; Borg, K.; De Visser, M.; Driessen, A.; Howard, R.; Nollet, F.; Opara, J.; Stalberg, E. EFNS Guideline on Diagnosis and Management of Post-polio Syndrome. Report of an EFNS Task Force. Euro J of Neurology 2006, 13, 795–801. [CrossRef]
  21. Rifai, N. Tietz Textbook of Laboratory Medicine; 7th ed.; Elsevier: Saint Louis, MO, 2022; ISBN 978-0-323-83467-4.
  22. World Health Organization Poliovirus Containment: Guidance to Minimize Risks for Facilities Collecting, Handling or Storing Materials Potentially Infectious for Polioviruses, Second Edition.; Second Edition.; WHO: Geneva, CH, 2021; ISBN ISBN 978-92-4-002121-1.
  23. Weldon, W.C.; Oberste, M.S.; Pallansch, M.A. Standardized Methods for Detection of Poliovirus Antibodies. In Poliovirus; Martín, J., Ed.; Methods in Molecular Biology; Springer New York: New York, NY, 2016; Vol. 1387, pp. 145–176 ISBN 978-1-4939-3291-7.
  24. Holick, M.F.; Binkley, N.C.; Bischoff-Ferrari, H.A.; Gordon, C.M.; Hanley, D.A.; Heaney, R.P.; Murad, M.H.; Weaver, C.M. Evaluation, Treatment, and Prevention of Vitamin D Deficiency: An Endocrine Society Clinical Practice Guideline. The Journal of Clinical Endocrinology & Metabolism 2011, 96, 1911–1930. [CrossRef]
  25. Shaghaghi, M.; Soleyman-jahi, S.; Abolhassani, H.; Yazdani, R.; Azizi, G.; Rezaei, N.; Barbouche, M.-R.; McKinlay, M.A.; Aghamohammadi, A. New Insights into Physiopathology of Immunodeficiency-Associated Vaccine-Derived Poliovirus Infection; Systematic Review of over 5 Decades of Data. Vaccine 2018, 36, 1711–1719. [CrossRef]
  26. Suares, J.E.; Khan, S.; Aadrika, A.; Poojari, P.G.; Rashid, M.; Thunga, G. Vaccine-Associated Paralytic Poliomyelitis in Oral Polio Vaccine Recipients: Disproportionality Analysis Using VAERS and Systematic Review. Expert Opinion on Drug Safety 2024, 23, 855–867. [CrossRef]
  27. Gilchrist, B.; Dolen, W.K. B Cell Disorders in Children—Part I. Curr Allergy Asthma Rep 2020, 20, 52. [CrossRef]
  28. Griffin, D.D.; Dolen, W.K. B Cell Disorders in Children: Part II. Curr Allergy Asthma Rep 2020, 20, 64. [CrossRef]
  29. Durandy, A.; Kracker, S.; Fischer, A. Primary Antibody Deficiencies. Nat Rev Immunol 2013, 13, 519–533. [CrossRef]
  30. Jones, T.P.W.; Buckland, M.; Breuer, J.; Lowe, D.M. Viral Infection in Primary Antibody Deficiency Syndromes. Reviews in Medical Virology 2019, 29. [CrossRef]
  31. Nimmerjahn, F.; Vidarsson, G.; Cragg, M.S. Effect of Posttranslational Modifications and Subclass on IgG Activity: From Immunity to Immunotherapy. Nat Immunol 2023, 24, 1244–1255. [CrossRef]
  32. Sun, L.; Kallolimath, S.; Palt, R.; Stiasny, K.; Mayrhofer, P.; Maresch, D.; Eidenberger, L.; Steinkellner, H. Increased in Vitro Neutralizing Activity of SARS-CoV-2 IgA1 Dimers Compared to Monomers and IgG. Proc. Natl. Acad. Sci. U.S.A. 2021, 118, e2107148118. [CrossRef]
  33. Song, P.; Zheng, N.; Liu, Y.; Tian, C.; Wu, X.; Ma, X.; Chen, D.; Zou, X.; Wang, G.; Wang, H.; et al. Deficient Humoral Responses and Disrupted B-Cell Immunity Are Associated with Fatal SFTSV Infection. Nat Commun 2018, 9. [CrossRef]
  34. Damelang, T.; Rogerson, S.J.; Kent, S.J.; Chung, A.W. Role of IgG3 in Infectious Diseases. Trends in Immunology 2019, 40, 197–211. [CrossRef]
  35. Kam, Y.-W.; Simarmata, D.; Chow, A.; Her, Z.; Teng, T.-S.; Ong, E.K.S.; Rénia, L.; Leo, Y.-S.; Ng, L.F.P. Early Appearance of Neutralizing Immunoglobulin G3 Antibodies Is Associated With Chikungunya Virus Clearance and Long-Term Clinical Protection. The Journal of Infectious Diseases 2012, 205, 1147–1154. [CrossRef]
  36. Baj, A.; Colombo, M.; Headley, J.L.; McFarlane, J.R.; Liethof, M.; Toniolo, A. Post-Poliomyelitis Syndrome as a Possible Viral Disease. International Journal of Infectious Diseases 2015, 35, 107–116. [CrossRef]
  37. Bianchi, F.P.; Larocca, A.M.V.; Bozzi, A.; Spinelli, G.; Germinario, C.A.; Tafuri, S.; Stefanizzi, P. Long-Term Persistence of Poliovirus Neutralizing Antibodies in the Era of Polio Elimination: An Italian Retrospective Cohort Study. Vaccine 2021, 39, 2989–2994. [CrossRef]
  38. Leroux-Roels, I.; Leroux-Roels, G.; Shukarev, G.; Schuitemaker, H.; Cahill, C.; De Rooij, R.; Struijs, M.; Van Zeeburg, H.; Jacquet, J.-M. Safety and Immunogenicity of a New Sabin Inactivated Poliovirus Vaccine Candidate Produced on the PER.C6® Cell-Line: A Phase 1 Randomized Controlled Trial in Adults. Human Vaccines & Immunotherapeutics 2021, 17, 1366–1373. [CrossRef]
  39. Martini, M.; Orsini, D. The Fight against Poliomyelitis through the History: Past, Present and Hopes for the Future. Albert Sabin’s Missing Nobel and His “Gift to All the World’s Children.” Vaccine 2022, 40, 6802–6805. [CrossRef]
  40. Sherf, R.M.; Cantrell, D.; Or, K.; Marcus, E.; Shapira, A.; Benbassat, C.; Ish-Shalom, S.; Koren, R. The Risk of Bone Fractures in Post-Poliomyelitis Patients Transitioning to Middle Adulthood. Endocrine Practice 2020, 26, 1277–1285. [CrossRef]
  41. Garceau, S.P.; Igbokwe, E.N.; Warschawski, Y.; Neufeld, M.E.; Safir, O.A.; Wade, J.P.; Guy, P.; Wolfstadt, J.I. Management Options and Outcomes for Patients with Femoral Fractures with Post-Polio Syndrome of the Lower Extremity: A Critical Analysis Review. JBJS Reviews 2020, 8, e0146–e0146. [CrossRef]
  42. Johnson, C.R.; Thacher, T.D. Vitamin D: Immune Function, Inflammation, Infections and Auto-Immunity. Paediatrics and International Child Health 2023, 43, 29–39. [CrossRef]
  43. Fischer, P.R.; Johnson, C.R.; Leopold, K.N.; Thacher, T.D. Treatment of Vitamin D Deficiency in Children. Expert Review of Endocrinology & Metabolism 2023, 18, 489–502. [CrossRef]
  44. Goldblum, N.; Gerichter, C.B.; Tulchinsky, T.H.; Melnick, J.L. Poliomyelitis Control in Israel, the West Bank and Gaza Strip: Changing Strategies with the Goal of Eradication in an Endemic Area. Bull World Health Organ 1994, 72, 783–796.
  45. Badizadegan, K.; Kalkowska, D.A.; Thompson, K.M. Health Economic Analysis of Antiviral Drugs in the Global Polio Eradication Endgame. Med Decis Making 2023, 43, 850–862. [CrossRef]
  46. Ianevski, A.; Frøysa, I.T.; Lysvand, H.; Calitz, C.; Smura, T.; Schjelderup Nilsen, H.-J.; Høyer, E.; Afset, J.E.; Sridhar, A.; Wolthers, K.C.; et al. The Combination of Pleconaril, Rupintrivir, and Remdesivir Efficiently Inhibits Enterovirus Infections in Vitro, Delaying the Development of Drug-Resistant Virus Variants. Antiviral Research 2024, 224, 105842. [CrossRef]
  47. Wilkinson, A.L.; Zaman, K.; Hoque, M.; Estivariz, C.F.; Burns, C.C.; Konopka-Anstadt, J.L.; Mainou, B.A.; Kovacs, S.D.; An, Q.; Lickness, J.S.; et al. Immunogenicity of Novel Oral Poliovirus Vaccine Type 2 Administered Concomitantly with Bivalent Oral Poliovirus Vaccine: An Open-Label, Non-Inferiority, Randomised, Controlled Trial. The Lancet Infectious Diseases 2023, 23, 1062–1071. [CrossRef]
  48. Kulkarni, P.S.; Zaman, K.; Desai, S.A.; Bharati, S.; Goswami, D.R.; Sharmeen, A.T.; Rana, S.; Haque, W.; Khandelwal, A.; Manney, S.; et al. Safety and Immunogenicity of a Reduced-Dose Inactivated Poliovirus Vaccine versus a Full-Dose Inactivated Poliovirus Vaccine in Infants in Bangladesh: A Double-Blind, Non-Inferiority, Randomised, Controlled, Phase 3 Trial. The Lancet Infectious Diseases 2025. [CrossRef]
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Figure 1. Levels of serum immunoglobulin G, A, and M in the study groups (mg/dL; median ± 95% CI). Numbers of subjects in each group are reported in the X axis labeling. Due to limitations in sample availability, not all planned tests were performed for every study participant, thus the numbers of subjects may vary among different assays. Statistically significant differences are indicated by p values.
Figure 1. Levels of serum immunoglobulin G, A, and M in the study groups (mg/dL; median ± 95% CI). Numbers of subjects in each group are reported in the X axis labeling. Due to limitations in sample availability, not all planned tests were performed for every study participant, thus the numbers of subjects may vary among different assays. Statistically significant differences are indicated by p values.
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Figure 2. Levels of serum immunoglobulin G subclasses in the study groups (mg/dL; median ± 95% CI). Numbers of subjects in each group are reported in the X axis labeling. Statistically significant differences are indicated by p values. N.S., not significant.
Figure 2. Levels of serum immunoglobulin G subclasses in the study groups (mg/dL; median ± 95% CI). Numbers of subjects in each group are reported in the X axis labeling. Statistically significant differences are indicated by p values. N.S., not significant.
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Figure 3. Neutralizing antibody titers to the three poliovirus serotypes in the study groups. Titers from 1:4 to 1:16,384 are reported (geometric mean ± 95% CI). Numbers of subjects in each group are reported in the X axis labeling. Statistically significant differences are indicated by p values.
Figure 3. Neutralizing antibody titers to the three poliovirus serotypes in the study groups. Titers from 1:4 to 1:16,384 are reported (geometric mean ± 95% CI). Numbers of subjects in each group are reported in the X axis labeling. Statistically significant differences are indicated by p values.
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Figure 4. Serum 25 hydroxy vitamin D levels in the study groups (nmol/L; median ± 95% CI). Numbers of subjects in each group are reported in the X axis labeling. Statistically significant differences are indicated by p values. N.S., not significant.
Figure 4. Serum 25 hydroxy vitamin D levels in the study groups (nmol/L; median ± 95% CI). Numbers of subjects in each group are reported in the X axis labeling. Statistically significant differences are indicated by p values. N.S., not significant.
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Figure 5. Distribution and interpretation of serum 25 hydroxy vitamin D (25(OH)D levels in healthy blood donors, family members of PPS subjects, PPS cases. Numbers of subjects in each group are reported in the X axis labeling. According to the Endocrine Society Clinical Practice Guideline on Vitamin D 17, serum 25(OH)D concentrations were interpreted as deficiency (≤50 nmol/L; Red), insufficiency (52.5-72.5 nmol/L; Yellow), and sufficiency (75-250 nmol/L; Green).
Figure 5. Distribution and interpretation of serum 25 hydroxy vitamin D (25(OH)D levels in healthy blood donors, family members of PPS subjects, PPS cases. Numbers of subjects in each group are reported in the X axis labeling. According to the Endocrine Society Clinical Practice Guideline on Vitamin D 17, serum 25(OH)D concentrations were interpreted as deficiency (≤50 nmol/L; Red), insufficiency (52.5-72.5 nmol/L; Yellow), and sufficiency (75-250 nmol/L; Green).
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Table 1. Demographic and clinical data of study groups.
Table 1. Demographic and clinical data of study groups.
Study groups
Parameters Healthy controls (blood donors) Family members of polio survivors Post-polio syndrome
Number of subjects 89 40 80
Percent female 46% 55.0% 57.5%
Percent polio vaccination (Salk or Sabin) 100% 57.7% 22.1%
Age (yrs) at medical visit and sample collection (median; IQR:Q1-Q3) 52.0; 42.0-58.5 49.0; 36.8-61.0 56.0; 51.8-62.0
Age (yrs) at diagnosis of APP (median; IQR:Q1-Q3) _ _ 2.0; 1.0-3.3
Age (yrs) at diagnosis of PPS (median; IQR:Q1-Q3) _ _ 49.0; 43.0-56.0
Note: APP, Acute Paralytic Poliomyelitis; PPS, Post-Polio Syndrome; IQR, Interquartile range.
Table 2. Immunoglobulin (Ig) levels lower than the cutoff values in the groups investigated.
Table 2. Immunoglobulin (Ig) levels lower than the cutoff values in the groups investigated.
Parameters Healthy controls (blood donors) Family members of polio survivors Post-polio syndrome
Ig levels below the lower reference range in the study groups (number/total, percentage).
IgG <600 mg/dL 0/50, 0% 6/29, 21% 10/80, 12%
IgA <80 mg/dL 1/50, 2% 7/29, 24% 8/80, 10%
IgM <40 mg/dL 1/50, 2% 3/29, 10% 7/80, 9%
IgG1 <380 mg/dL 1/50, 0% 7/29, 24% 18/80, 22%
IgG2 <120 mg/dL 0/50, 0% 2/29, 7% 3/80, 4%
IgG3 <18 mg/dL 0/50, 0% 10/29, 34% 22/80, 27%
IgG4 <18 mg/dL 1/50, 2% 3/29, 10% 10/80, 12%
Note. Ig levels: reference ranges for adult Caucasians have been used (Rifai 2022). Limits for significantly low Ig levels have been validated at our own laboratory (Ospedale di Circolo, Varese, Italy) using a cohort of 120 healthy adult blood donors (median age 51.2 ± 11.4 years). The obtained intervals encompass ≥95% of the values found in the reference group.
Table 3. Non-protective serum titers of poliovirus-neutralizing antibodies (PV NAb) in the groups investigated.
Table 3. Non-protective serum titers of poliovirus-neutralizing antibodies (PV NAb) in the groups investigated.
Parameters Healthy controls (blood donors) Family members of polio survivors Post-polio syndrome
Polio vaccination rate - Number/total, percentage 30/30, 100% 21/38, 55.3% 16/75, 21.3%
Non protective serum titers (<1:8) of poliovirus-neutralizing antibodies in the study groups (number/total, percentage).
PV1 NAb titer <1:8 0/30, 0% 1/38, 2.6% 5/75, 6.7%
PV2 NAb titer <1:8 0/30, 0% 1/38, 2.6% 8/75, 10.7%
PV3 NAb titer <1:8 0/30, 0% 0/38, 0% 7/75, 9.3%
Note. Eight replicates were used for evaluating poliovirus NAb titers. PV Nab titers were calculated using the Reed-Muench formula and are the only measurement known to correlate with protection from PV infection. Titers <1:8 are considered non-protective.
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