key: cord-0955873-agre2iwp
authors: Latifi-Pupovci, Hatixhe; Namani, Sadie; Pajaziti, Artina; Ahmetaj-Shala, Blerina; Ajazaj, Lindita; Kotori, Afrim; Haxhibeqiri, Valdete; Gegaj, Valentin; Bunjaku, Gramoz
title: Relationship of anti-SARS-CoV-2 IgG antibodies with Vitamin D and inflammatory markers in COVID-19 patients
date: 2022-04-05
journal: Sci Rep
DOI: 10.1038/s41598-022-09785-7
sha: cdd4e2965a02fb6326e52f38efa918b390e16c93
doc_id: 955873
cord_uid: agre2iwp

Several studies have found an association of COVID-19 disease severity with Vitamin D deficiency and higher levels of anti-SARS-CoV-2 IgGs. The aim of this study was to determine whether levels of Vitamin D and “inflammatory state” influence the magnitude of anti-SARS-CoV-2 IgGs levels in COVID-19 patients. For this purpose, in 67 patients levels of anti-SARS-CoV-2 IgG were measured in week 4 whereas in 52 patients levels of Vitamin D were measured in week 1 after symptom onset. We found that low Vitamin D levels were significantly associated with age and disease severity whereas there was a trend without significance, towards negative correlation of Vitamin D with anti-SARS-CoV-2 IgG. Anti-SARS-CoV-2 IgG were significantly higher in older ages, patients with severe disease, diabetes and those who received corticosteroid and antibiotic therapy. There was a positive correlation of anti-SARS-CoV-2 IgG with IL-6, CRP, LDH, ESR and with percentages of granulocytes. In conclusion, Vitamin D and anti-SARS-CoV-2 IgG share common parameters associated with inflammatory state. However, even though Vitamin D protects against severe forms of COVID-19 it could not directly affect anti-SARS-CoV-2 IgG production.

A total of 69 patients diagnosed with COVID-19 were enrolled in this study. The median age of patients was 59 years (44.5-67.0 years) of whom 53.6% were females and 46.4% males. Patient characteristics are presented in Table 1 .

We investigated the factors that are likely to influence anti-SARS-CoV-2 IgG levels in COVID-19 patients. We found that age, but not gender, significantly influenced IgG levels in this group of patients. Specifically, patients aged > 50 were found to have significantly higher IgG levels than patients < 50 (Fig. 1 ). When grouping according to disease severity the distribution of IgG-w4 was different across categories of disease severity. Mean ranks of anti-SARS-CoV-2 IgG were significantly higher in patients with diabetes and those who received corticosteroid and antibiotic therapy (Fig. 1) . IgG levels were also higher in patients with hypertension but this did not reach significance (p = 0.054).

Vit. D is associated with age and disease severity. Next, we sought to determine whether the magnitude of anti-SARS-CoV-2 IgG antibody level was related to Vit. D levels. In 65.4% of 52 patients, levels of Vit. D were below normal values. Gender did not influence Vit. D, however once again, age was significantly correlated with Vit. D. A significant difference in distribution of Vit. D was also found in different groups of patients according to disease severity and outcome (Fig. 2) ; all deceased patients were insufficient, 75% of them being VDD.

To determine other factors that are likely to influence anti-SARS-CoV-2 IgG production and the relationship of Vit. D with these factors, we did a correlation analysis of anti-SARS-CoV-2 IgG and Vit. D with inflammatory and hematological markers in the first week post-symptom onset (PSO) and with the most changed values (maximum values of CRP, D-Dimer, LDH, ESR, percentages of granulocytes and minimum values of WBC count, platelet count, percentages of monocyte and percentages of lymphocytes) during the course of disease. Anti-SARS-CoV-2 IgG were positively correlated with IL-6, CRP, LDH, ESR and percentages of granulocytes determined in the first week PSO (Table 2) . On the other hand, levels of IgG were weakly correlated with percentages of lymphocytes, but without significance. When analysed with the most changed values during the course of disease, we found stronger negative correlation between anti-SARS-CoV-2 with maximum values of CRP, LDH, ESR and percentages of granulocyte than with parameters found in the first week PSO. When we analysed correlations between Vit. D and various inflammatory and hematological parameters, in the first week PSO we found a significant negative correlation between the Vit. D and IL-6, CRP, D-dimer, ESR and a significant positive correlation with platelet count. When we analysed correlation of Vit.D with the most Figure 1 . Distribution of anti-SARS-CoV-2 IgG across age groups, disease severity groups, patients with and without diabetes, corticosteroid and antibiotic administration. Levels of IgG were significantly higher in age group > 50, severe and critical patients, in diabetics and patients treated with corticosteroids and antibiotics. www.nature.com/scientificreports/ changed laboratory parameters during the course of disease, stronger negative correlation was found between Vit. D and CRP, D-Dimer, ESR and platelet count than with these parameters in the first week PSO whereas a negative correlation was found also with minimum values of WBC count. There was a negative correlation of IgG-w4 with Vit. D-w1, however this did not reach statistical significance (p = 0.296) ( Table 2) .

In order to estimate the change of Vit. D during illness and the change of anti-SARS-CoV-2 IgG after 3 months, we compared median differences in paired samples (Vit. D-w1 and Vit. D-w4; IgG-w4 and IgG-m4). In 66% of patients (N = 50) levels of Vit. D decreased during the illness although all patients were supplemented with Vit. D; hospitalised patients were supplemented with 4000 UI/ml, whereas ambulatory patients took no more than 1000 UI/ml. There were no significant differences in Vit. D decrease during illness between groups of patients by sex, age, disease severity and comorbidity ( Table 3) .

The changes of IgG levels between two measurements were analysed in 17 patients. In 6 patients we found an increase of IgG levels, whereas in 11 we found a decrease of antibody levels. There was a significant difference in anti-SARS-CoV-2 decrease between groups of patients according to disease severity, with higher reduction of IgG levels in severe patients (Table 3) .

This is, to our knowledge, the first report analysing the Vit. D status and magnitude of anti-SARS-CoV-2 IgG antibody production in COVID-19 patients. Although in our study baseline levels of Vit. D were below normal values in 65.4% of patients, these values were in agreement with other publications [36] [37] [38] . We show that Vit. D distribution was affected by age and disease severity, but not sex. Similar findings were described in several other studies [39] [40] [41] [42] . Ilie et al. also showed a negative correlation between Vit. D levels and COVID-19 cases and mortality 8 . A meta-analysis with a total of 1368 COVID-19 patients also showed that low Vit. D levels were significantly associated with poorer patient outcome and prognosis 42 . In contrast Hastie et al. found no link between Vit. D and risk of severe COVID-19 infection and mortality in 341,484 UK Biobank participants 43 .

Vit. D has well recognised immunoregulatory actions; it reduces production of pro-inflammatory cytokines (IL-6, IL-8 and IL-17) and increases anti-inflammatory cytokines (IL-10) leading to down-regulation of TH1 cells and up-regulation of TH2 cells 14 . It is therefore assumed that VDD could be a central factor in 'cytokine storm' seen in COVID-19 infection; patients with low concentrations of Vit. D (≤ 30 nmol/l or ≤ 12 ng/ml) have demonstrated significant, elevated markers of cytokine storm 44 . In this study we found a significant negative correlation between Vit. D levels and various inflammatory markers including IL-6, CRP, ESR and D-dimer. Despite observing trends, albeit not significant, Carpagnano et al. found higher levels of IL-6 in COVID patients with Table 2 . Mutual correlation between IgG-w4 and Vit. D-w1 and correlation between these parameters and inflammatory and hematological markers. Spearman correlation and significance. www.nature.com/scientificreports/ severe VDD 45 . IL-6 also plays a key role in cytokine storm and induces rise of CRP 46 , a well known inflammatory marker that also significantly increases in severe forms of COVID-19 47, 48 . Since IL-6 bioactivity may change in the presence of Vit. D, CRP may be a more accurate indicator of pro-inflammatory cytokines than IL-6 46 . Several studies, which are in line with our study, have shown an inverse association between Vit. D and CRP 14, 21 .

In COVID-19, virus-specific B-cell mediated humoral immunity has been implicated and majority of patients seroconverted during recovery phase. In this study 97% of patients seroconverted with higher IgG levels in males than in females, but with no significant difference. The same results were found by Kutsuna et al. but they reported a significant difference for the fact that in that study significance was set at p = 0.1 32 . Also Robbiani et al. reported higher anti-SARS-CoV-2 IgG in men than in women 49 . Age distribution of anti-SARS-CoV-2 IgG in this study was significantly different between the groups, with higher levels in patients > 50 years. This finding is in line with other studies 50, 51 .

Our results confirm previous findings that clinical COVID-19 disease severity is associated with higher anti-SARS-CoV-2 serum-IgG antibodies 27,32 although To et al. found that elevated antibody titers do not correlate with the severity of disease 52 . The exact immune mechanisms responsible for different IgG responses between different forms of disease are not known. Whereas Gozalbo-Rovira et al. 18 reported that patients with severe forms of the disease could be exposed to higher and more perdurable viral burdens, Hoepel et al. suggest that worsening of disease during SARS-CoV-2 infection could be caused by antibodies 53 . Gao et al. found that moderate and severe symptomatic patients exhibited a significant increase in frequencies of B-cells compared to healthy controls 54 . This demonstrates that compared with potent SARS-CoV-2-specific B cell responses mounted in COVID-19 patients after moderate or severe illness, asymptomatic or mild symptomatic COVID-19 patients only induced weak and transient SARS-CoV-2-specific B cell responses 54 .

By analysing anti-SARS-CoV-2 IgG in relation to comorbidities, significantly different distribution was found among patients with and without diabetes but not with and without hypertension, results similar to Kutsuna et al. 32 . Esperança-Martins et al. found significantly lower levels of anti-SARS-CoV-2 IgG in cancer patients 55 , a finding we could not corroborate possibly due to the low number of cancer patients recruited in the study. With regard to therapies, our finding that corticosteroid use and IgG-w4 were associated were similar to findings by Kutsuna et al. 32 . This association may be a result of the use of corticosteroids in moderate and severe patients, which already showed a relationship with IgG levels.

In this study we sought to determine whether the magnitude of SARS-CoV-2 response was related to an inflammatory state. Correlation analyses show that anti-SARS-CoV-2 IgGs were significantly correlated with IL-6, CRP, ESR, LDH, lower WBC count, higher persentages of granulocytes, lower persentages of lymphocytes and www.nature.com/scientificreports/ lower persentages of monocytes. Gozalbo-Rovira et al. also found weak or very weak correlation of anti-RBD-IgG with inflammatory markers such as CRP, IL-6, D-Dimer and LDH 18 . Corrrelation between anti-SARS-CoV-2 antibodies and CRP levels were reported also by other authors 32, 56, 57 . Correlation of anti-SARS-CoV-2 antibodies with LDH levels found in first week PSO and maximum values during the disease are in line with Kutsuna et al. 32 . Increase in neutrophil count and decrease in the lymphocytes were more common in severe cases than in moderate cases of COVID-19 58, 59 and indicate the intensity of inflammatory response. In this study we found that the maximum values of granulocytes and minimum values of lymphocytes during the course of disease are in correlation with anti-SARS-Cov-2 IgG which are olso found to be higher in severe cases of disease who also showed higher inflammatory responses. The same was found by Gozalbo-Rovira et al. 18 .

A key question of this study was if baseline Vit. D levels may influence the serological response in patients with COVID-19. Similar to our findings, Yonghong et al. in 18,148 individuals found that SARS-CoV-2 seropositivity was not associated with having a Vit. D level less than 30 ng/ml before or during the pandemic independently of other risk factors 38 . Also Barassi et al. reported that there was no relationship between Vit. D and anti-SARS-CoV-2 IgG values 60 . Although Kaufman et al. found strong and inverse association between Vit. D and SARS-CoV-2 positivity, in contrast to our study they did not carry out quantitative analyses between these parameters 35 .

Prior studies reported that SARS-Cov-2 IgG levels decline during time post infection 61,62 and the same was found in this study in which in 65% of patients with measured IgG-m4, levels of IgG decreased after three months. A significant difference in decrease of SARS-CoV-2 IgG was found between groups of patients according to disease severity, with higher reduction of IgG levels in severe patients. Our results are in line with the results of Kutsuna et al. in which in moderate and severely ill patients titers of IgG tended to decline 60 days PSO compared to mild cases 32 . Ma et al. analysed decline rate of IgG and predicted convalescent patients' SARS-CoV-2 IgG to be undetectable approximately 273 days after hospital discharge 63 . This study has some limitations. First, the sample size of this study is modest and not all patients had all laboratory analyses completed making paired analysis difficult. The second limitation of the study was the collection of samples at different sites.

In summary, anti-SARS-CoV-2 IgGs and Vit. D shares common parameters associated with inflammatory state. This could lead us to suppose that Vit. D signaling, targeting several immune-mediated pathways, protects against severe forms of COVID-19 but it does not directly affect the anti-SARS-CoV-2 IgG production. However, further work needs to be completed to address whether Vit. D influences serological response in COVID-19 patients. 

Anti-SARS-CoV-2 IgG antibodies levels were determined using the SARS-CoV-2 IgG II Quant assay, an quantitative chemiluminescent microparticle immunoassay (CMIA), (Abbott) according to the manufacturer's instructions. The cut-off value for test positivity was 50.0 AU/ml with analytical measurement interval of 21-40,000 AU/ml. In 67 of 69 patients (as mentioned above, two passed away before week 4) anti-SARS-CoV-2 IgG antibodies were measured at week 4 since symptom onset (IgG-w4; n = 67). In 17 of these patients, IgG levels were also measured at 4 months since symptom onset (IgG-m4; n = 17).

Clinical parameters. Additional information was collected from recruited patients including, age, sex, illness severity, comorbidities, medications used to treat illness, clinical outcome, inflammatory markers (IL-6, CRP, D-dimer and LDH), hematological parameters [Erythrocyte Sedimantatio Rate (ESR), White Blood Cell count (WBC), percentages of granulocytes, lymphocytes and monocytes and platelet count] during acute phase of COVID-19.

Statistical analysis. Data www.nature.com/scientificreports/ were expressed as medians and inter-quartile ranges. Chi-Square test was used to examine relationships between categorical variables. Due to non-normal distribution of data, comparisons across disease severity categories and age groups were conducted using Kruskal-Wallis test; Mann-Whitney U Test was used for comparisons accross two categorical independent goups (sex and hospitalisation); whereas comparison accross positive and negative ranks was carried out by using Wilcoxon Signed-Rank Test. Spearman's rank correlation coefficient was used to gauge monotonic relationship between Vitamin D and IgG levels, as well as inflammatory and hematological markers. Statistical analyses were carried out with SPSS (version 25) and/or Graphpad Prism v9.0. All tests were 2-talied and P-values < 0.05 were considered significant.

Ethics declaration. This study was approved by the Ethics Committee at University Clinical Centre of Kosova (reference no 2548/2020). Written informed consent was obtained from all participants, in accordance with the Declaration of Helsinki.

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation. www.nature.com/scientificreports/

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The authors gratefully acknowledge the assistance of midwife Arlinda Fushtica, Dr. Luljeta Hasani and Dr. Albina Ponosheci-Biçaku for help in providing patients blood samples at the Infectious Diseases Clinic.

The authors declare no competing interests.

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