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A Rapid Ecologic Analysis, Confirmed by a Case-control Study, Identifies Class I HLA Alleles Correlated to the Risk of COVID-19

Abstract

Background: Several studies suggest that the heterogeneous spread of SARS-CoV-2 pandemics started on December 2019 could be partially upheld by the prevalence of permissive class I HLA alleles in specific populations. Such HLA alleles are in fact unable to shape an efficient anti-viral immune-response in the hosts or sustain an exaggerated inflammatory T cell mediated response responsible for the COVID-19 disease. We previously reported an ecologic correlation between the risk of COVID-19 spreading across Italy and the germinal expression of permissive HLA-C*01 and -B*44 alleles in specific inter and intraregional populations along the first spreading wave.

Methods: Considering that SARS-CoV-2 has undergone multiple adaptative mutations since the beginning of pandemics related to a natural immunization and to the worldwide campaign of anti-SARS-CoV-2 vaccination, we have carried out further analyses to evaluate whether the predictive value of class I HLA-allele gene prevalence and COVID-19 incidence has changed with time along the first four pandemics spreading waves in Italy. To this purpose we carried out an ecologic study followed by a case-control study.

Results: | Our data revealed that the direct correlation of HLA-C*01, and HLA-B*44 gene expression and COVID-19 risk was completely lost just after the first pandemics wave in Italy. On the contrary, the expression of HLA-B*49 allele in specific populations emerged as inversely correlated to the risk of COVID-19 and could be considered as a protective factor. The statistical significance of this correlation was progressively enforced in each subsequent spreading wave until February 2022. The following case-control study in the two Regions of Campania and Calabria in Italy confirmed the protective value of HLA-B*49 allele gene expression (OR = 0.289; p = 0.041), although statistical significance is lost after adjustment by logistic regression model. The analysis also detected multiple class I HLA-alleles whose expression was strongly correlated with COVID-19 risk: HLA-B*08 (OR = 3.193; p = 0.015); -B*14:01 (OR = 3.596; p = 0.018); -B*15:01 (OR = 5.124; p = 0.001); -B*35 (OR = 2.972; p = 0.002).

Conclusions: Our study not only identifies specific HLA alleles related to COVID-19 risk but also exemplifies a rapid and inexpensive approach that can be used to identify individuals needing prioritization during vaccination campaigns.

References
1.
Vejbaesya S, Thongpradit R, Kalayanarooj S, Luangtrakool K, Luangtrakool P, Gibbons R . HLA Class I Supertype Associations With Clinical Outcome of Secondary Dengue Virus Infections in Ethnic Thais. J Infect Dis. 2015; 212(6):939-47. PMC: 4548457. DOI: 10.1093/infdis/jiv127. View

2.
Nguyen A, David J, Maden S, Wood M, Weeder B, Nellore A . Human Leukocyte Antigen Susceptibility Map for Severe Acute Respiratory Syndrome Coronavirus 2. J Virol. 2020; 94(13). PMC: 7307149. DOI: 10.1128/JVI.00510-20. View

3.
Grams S, Moonsamy P, Mano C, Oksenberg J, Begovich A . Two new HLA-B alleles, B*4422 and B*4704, identified in a study of families with autoimmunity. Tissue Antigens. 2002; 59(4):338-40. DOI: 10.1034/j.1399-0039.2002.590417.x. View

4.
Correale P, Mutti L, Pentimalli F, Baglio G, Saladino R, Sileri P . HLA-B*44 and C*01 Prevalence Correlates with Covid19 Spreading across Italy. Int J Mol Sci. 2020; 21(15). PMC: 7432860. DOI: 10.3390/ijms21155205. View

4.
Ni P, Clinkenbeard E, Noonan M, Richardville J, McClintick J, Hato T . Targeting fibroblast growth factor 23-responsive pathways uncovers controlling genes in kidney mineral metabolism. Kidney Int. 2020; 99(3):598-608. PMC: 7914218. DOI: 10.1016/j.kint.2020.10.024. View