HLA-DR polymorphism in SARS-CoV-2 infection and susceptibility to symptomatic COVID-19

Stuart Astbury, Catherine J Reynolds, David K Butler, Diana C Muñoz-Sandoval, Kai-Min Lin, Franziska P Pieper, Ashley Otter, Afroditi Kouraki, Lola Cusin, Jessica Nightingale, Amrita Vijay, Simon Craxford, Guruprasad P Aithal, Patrick J Tighe, Joseph M Gibbons, Corinna Pade, George Joy, Mala Maini, Benny Chain, Amanda Semper, Timothy Brooks, Benjamin J Ollivere, Áine McKnight, Mahdad Noursadeghi, Thomas A Treibel, Charlotte Manisty, James C Moon, COVIDsortium Investigators*, Ana M Valdes, Rosemary J Boyton, Daniel M Altmann, Hakam Abbass, Aderonke Abiodun, Mashael Alfarih, Zoe Alldis, Daniel M Altmann, Oliver E Amin, Mervyn Andiapen, Jessica Artico, João B Augusto, Georgiana L Baca, Sasha N L Bailey, Anish N Bhuva, Alex Boulter, Ruth Bowles, Rosemary J Boyton, Olivia V Bracken, Ben O'Brien, Tim Brooks, Natalie Bullock, David K Butler, Gabriella Captur, Nicola Champion, Carmen Chan, Aneesh Chandran, David Collier, Jorge Couto de Sousa, Xose Couto-Parada, Teresa Cutino-Moguel, Rhodri H Davies, Brooke Douglas, Cecilia Genova, Keenan Dieobi-Anene, Mariana O Diniz, Anaya Ellis, Karen Feehan, Malcolm Finlay, Marianna Fontana, Nasim Forooghi, Celia Gaier, Joseph M Gibbons, Derek Gilroy, Matt Hamblin, Gabrielle Harker, Jacqueline Hewson, Lauren M Hickling, Aroon D Hingorani, Lee Howes, Alun Hughes, Gemma Hughes, Rebecca Hughes, Ivie Itua, Victor Jardim, Wing-Yiu Jason Lee, Melaniepetra Jensen, Jessica Jones, Meleri Jones, George Joy, Vikas Kapil, Hibba Kurdi, Jonathan Lambourne, Kai-Min Lin, Sarah Louth, Mala K Maini, Vineela Mandadapu, Charlotte Manisty, Áine McKnight, Katia Menacho, Celina Mfuko, Oliver Mitchelmore, Christopher Moon, James C Moon, Diana C Muñoz-Sandoval, Sam M Murray, Mahdad Noursadeghi, Ashley Otter, Corinna Pade, Susana Palma, Ruth Parker, Kush Patel, Babita Pawarova, Steffen E Petersen, Brian Piniera, Franziska P Pieper, Daniel Pope, Mary Prossora, Lisa Rannigan, Alicja Rapala, Catherine J Reynolds, Amy Richards, Matthew Robathan, Joshua Rosenheim, Genine Sambile, Nathalie M Schmidt, Amanda Semper, Andreas Seraphim, Mihaela Simion, Angelique Smit, Michelle Sugimoto, Leo Swadling, Stephen Taylor, Nigel Temperton, Stephen Thomas, George D Thornton, Thomas A Treibel, Art Tucker, Jessry Veerapen, Mohit Vijayakumar, Sophie Welch, Theresa Wodehouse, Lucinda Wynne, Dan Zahedi, Daniel M Altmann, Rosemary J Boyton, Tim Brooks, Benjamin Chain, Mala K Maini, Charlotte Manisty, Áine McKnight, James C Moon, Mahdad Noursadeghi, Thomas A Treibel, Guruprasad P Aithal, Waheed Ashraf, Stuart Astbury, Jonathan K Ball, Joseph G Chappell, Simon Craxford, Lola M L Cusin, Joshua D Duncan, Adeel Ikram, William L Irving, Hannah J Jackson, Anthony Kelly, Melanie Lingaya, Ben A Marson, Jayne Newham, Jessica Nightingale, Alan Norrish, Barbara Nowicka, Benjamin J Ollivere, Alexander W Tarr, Patrick J Tighe, Theocharis Tsoleridis, Richard A Urbanowicz, Ana M Valdes, Amrita Vijay, Stuart Astbury, Catherine J Reynolds, David K Butler, Diana C Muñoz-Sandoval, Kai-Min Lin, Franziska P Pieper, Ashley Otter, Afroditi Kouraki, Lola Cusin, Jessica Nightingale, Amrita Vijay, Simon Craxford, Guruprasad P Aithal, Patrick J Tighe, Joseph M Gibbons, Corinna Pade, George Joy, Mala Maini, Benny Chain, Amanda Semper, Timothy Brooks, Benjamin J Ollivere, Áine McKnight, Mahdad Noursadeghi, Thomas A Treibel, Charlotte Manisty, James C Moon, COVIDsortium Investigators*, Ana M Valdes, Rosemary J Boyton, Daniel M Altmann, Hakam Abbass, Aderonke Abiodun, Mashael Alfarih, Zoe Alldis, Daniel M Altmann, Oliver E Amin, Mervyn Andiapen, Jessica Artico, João B Augusto, Georgiana L Baca, Sasha N L Bailey, Anish N Bhuva, Alex Boulter, Ruth Bowles, Rosemary J Boyton, Olivia V Bracken, Ben O'Brien, Tim Brooks, Natalie Bullock, David K Butler, Gabriella Captur, Nicola Champion, Carmen Chan, Aneesh Chandran, David Collier, Jorge Couto de Sousa, Xose Couto-Parada, Teresa Cutino-Moguel, Rhodri H Davies, Brooke Douglas, Cecilia Genova, Keenan Dieobi-Anene, Mariana O Diniz, Anaya Ellis, Karen Feehan, Malcolm Finlay, Marianna Fontana, Nasim Forooghi, Celia Gaier, Joseph M Gibbons, Derek Gilroy, Matt Hamblin, Gabrielle Harker, Jacqueline Hewson, Lauren M Hickling, Aroon D Hingorani, Lee Howes, Alun Hughes, Gemma Hughes, Rebecca Hughes, Ivie Itua, Victor Jardim, Wing-Yiu Jason Lee, Melaniepetra Jensen, Jessica Jones, Meleri Jones, George Joy, Vikas Kapil, Hibba Kurdi, Jonathan Lambourne, Kai-Min Lin, Sarah Louth, Mala K Maini, Vineela Mandadapu, Charlotte Manisty, Áine McKnight, Katia Menacho, Celina Mfuko, Oliver Mitchelmore, Christopher Moon, James C Moon, Diana C Muñoz-Sandoval, Sam M Murray, Mahdad Noursadeghi, Ashley Otter, Corinna Pade, Susana Palma, Ruth Parker, Kush Patel, Babita Pawarova, Steffen E Petersen, Brian Piniera, Franziska P Pieper, Daniel Pope, Mary Prossora, Lisa Rannigan, Alicja Rapala, Catherine J Reynolds, Amy Richards, Matthew Robathan, Joshua Rosenheim, Genine Sambile, Nathalie M Schmidt, Amanda Semper, Andreas Seraphim, Mihaela Simion, Angelique Smit, Michelle Sugimoto, Leo Swadling, Stephen Taylor, Nigel Temperton, Stephen Thomas, George D Thornton, Thomas A Treibel, Art Tucker, Jessry Veerapen, Mohit Vijayakumar, Sophie Welch, Theresa Wodehouse, Lucinda Wynne, Dan Zahedi, Daniel M Altmann, Rosemary J Boyton, Tim Brooks, Benjamin Chain, Mala K Maini, Charlotte Manisty, Áine McKnight, James C Moon, Mahdad Noursadeghi, Thomas A Treibel, Guruprasad P Aithal, Waheed Ashraf, Stuart Astbury, Jonathan K Ball, Joseph G Chappell, Simon Craxford, Lola M L Cusin, Joshua D Duncan, Adeel Ikram, William L Irving, Hannah J Jackson, Anthony Kelly, Melanie Lingaya, Ben A Marson, Jayne Newham, Jessica Nightingale, Alan Norrish, Barbara Nowicka, Benjamin J Ollivere, Alexander W Tarr, Patrick J Tighe, Theocharis Tsoleridis, Richard A Urbanowicz, Ana M Valdes, Amrita Vijay

Abstract

SARS-CoV-2 infection results in different outcomes ranging from asymptomatic infection to mild or severe disease and death. Reasons for this diversity of outcome include differences in challenge dose, age, gender, comorbidity and host genomic variation. Human leukocyte antigen (HLA) polymorphisms may influence immune response and disease outcome. We investigated the association of HLAII alleles with case definition symptomatic COVID-19, virus-specific antibody and T-cell immunity. A total of 1364 UK healthcare workers (HCWs) were recruited during the first UK SARS-CoV-2 wave and analysed longitudinally, encompassing regular PCR screening for infection, symptom reporting, imputation of HLAII genotype and analysis for antibody and T-cell responses to nucleoprotein (N) and spike (S). Of 272 (20%) HCW who seroconverted, the presence of HLA-DRB1*13:02 was associated with a 6·7-fold increased risk of case definition symptomatic COVID-19. In terms of immune responsiveness, HLA-DRB1*15:02 was associated with lower nucleocapsid T-cell responses. There was no association between DRB1 alleles and anti-spike antibody titres after two COVID vaccine doses. However, HLA DRB1*15:01 was associated with increased spike T-cell responses following both first and second dose vaccination. Trial registration: NCT04318314 and ISRCTN15677965.

Keywords: COVID-19; HLA; SARS-CoV-2; T-cell immunity; immunogenetics; vaccine.

Conflict of interest statement

R.J.B. and D.M.A. are members of the Global T cell Expert Consortium and have consulted for Oxford Immunotec outside the submitted work.

© 2022 The Authors. Immunology published by John Wiley & Sons Ltd.

Figures

FIGURE 1
FIGURE 1
Association between HLA DRB1 alleles, the presence of case definition symptoms and T cell immune responses to SARS‐CoV‐2 following natural infection: (a) consistent association of DRB1*13:02 with the presence of case definition symptoms; (b) Association between the absence of HLA‐DRB1*15:02 and T‐cell responses against nucleoprotein peptide pool (HLA‐DRB1*15:02 −, n = 68, HLA‐DRB1*15:02 +, n = 5). Bars show mean with SD. P value calculated using a Mann–Whitney U test. PBMC for T cell assays were taken on average 121 (range 71–174) days following first presentation of case definition symptoms. HLA, human leukocyte antigen; PBMC, peripheral blood mononuclear cells
FIGURE 2
FIGURE 2
HLA DRB1 alleles not associated with enhanced antibody responses but DR15:01 associated with higher T cell responses to spike in prior SARS‐CoV‐2 infected HCW: (a) Anti‐spike titres after two doses of COVID vaccine were evaluated in the context of the top 12 most frequent DR alleles in HCW from the COVIDsortium (n = 251) and PANTHER (n = 169) cohorts. (b–d) Association between the presence of the DRB1*1501 allele and T‐cell responses against (b) spike protein in single dose vaccinated HCW, (c) spike peptide pool in single dose vaccinated HCW and (d) spike peptide pool in two dose vaccinated HCW with prior SARS‐Co‐V‐2 infection (upper panel, n = 23) and SARS‐CoV‐2 naïve vaccinees (lower panel, n = 23). P values were calculated using a Mann‐Whitney U test. Data are shown as box and whisker plots. HCW, healthcare worker; HLA, human leukocyte antigen

References

    1. Pairo‐Castineira E, Clohisey S, Klaric L, Bretherick AD, Rawlik K, Pasko D, et al. Genetic mechanisms of critical illness in COVID‐19. Nature. 2021;591:92–8.
    1. Severe Covid‐19 GWAS Group , Ellinghaus D, Degenhardt F, Bujanda L, Buti M, Albillos A, et al. Genomewide association study of severe COVID‐19 with respiratory failure. N Engl J Med. 2020. Oct 15;383(16):1522–34.
    1. Alghamdi J, Alaamery M, Barhoumi T, Rashid M, Alajmi H, Aljasser N, et al. Interferon‐induced transmembrane protein‐3 genetic variant rs12252 is associated with COVID‐19 mortality. Genomics. 2021. Apr 7;113:1733–41.
    1. Zhang Q, Bastard P, Liu Z, et al. Inborn errors of type I IFN immunity in patients with life‐threatening COVID‐19. Science. 2020;370:eabd4570.
    1. Blackwell JM, Jamieson SE, Burgner D. HLA and infectious diseases. Clin Microbiol Rev. 2009;22:370–85.
    1. Hill AVS. Evolution, revolution and heresy in the genetics of infectious disease susceptibility. Philos Trans R Soc Lond B Biol Sci. 2012;367:840–9.
    1. Martin MP, Carrington M. Immunogenetics of HIV disease. Immunol Rev. 2013;254:245–64. 10.1111/imr.12071
    1. Singh R, Kaul R, Kaul A, Khan K. A comparative review of HLA associations with hepatitis B and C viral infections across global populations. World J Gastroenterol. 2007;13:1770–87.
    1. Davidson EJ, Davidson JA, Sterling JC, Baldwin PJW, Kitchener HC, Stern PL. Association between human leukocyte antigen polymorphism and human papillomavirus 16‐positive vulval intraepithelial neoplasia in British women. Can Res. 2003;63:400–40.
    1. Tian C, Hromatka BS, Kiefer AK, Eriksson N, Noble SM, Tung JY, et al. Genome‐wide association and HLA region fine‐mapping studies identify susceptibility loci for multiple common infections. Nat Commun. 2017;8(1):599.
    1. Dendrou CA, Petersen J, Rossjohn J, Fugger L, et al. HLA variation and disease. Nat Rev Immunol. 2018;18:325–39.
    1. Ovsyannikova IG, Jacobson RM, Poland GA. Variation in vaccine response in normal populations. Pharmacogenomics. 2004;5:417–27.
    1. Ovsyannikova IG, Pankratz VS, Vierkant RA, Pajewski NM, Quinn CP, Kaslow RA, et al. Human leukocyte antigens and cellular immune responses to anthrax vaccine adsorbed. Infect Immun. 2013;81:2584–91.
    1. Horton R, Wilming L, Rand V, Lovering RC, Bruford EA, Khodiyar VK, et al. Gene map of the extended human MHC. Nat Rev Genet. 2004;5:889–99.
    1. Treibel TA, Manisty C, Burton M, McKnight Á, Lambourne J, Augusto JB, et al. COVID‐19: PCR screening of asymptomatic health‐care workers at London hospital. Lancet. 2020;395:1608–10. 10.1016/S0140-6736(20)31100-4
    1. Augusto JB, Menacho K, Andiapen M, Bowles R, Burton M, Welch S, et al. Healthcare workers bioresource: study outline and baseline characteristics of a prospective healthcare worker cohort to study immune protection and pathogenesis in COVID‐19. Wellcome Open Res. 2020;5:179. 10.12688/wellcomeopenres.16051.2.
    1. Manisty C, Treibel TA, Jensen M, Semper A, Joy G, Gupta RK, et al. Time series analysis and mechanistic modelling of heterogeneity and sero‐reversion in antibody responses to mild SARS‐CoV‐2 infection. EBioMedicine. 2021;65:103259.
    1. Valdes AM, Moon JC, Vijay A, Chaturvedi N, Norrish A, Ikram A, et al. Longitudinal assessment of symptoms and risk of SARS‐CoV‐2 infection in healthcare workers across 5 hospitals to understand ethnic differences in infection risk. EClinicalMedicine. 2021;34:100835.
    1. Reynolds CJ, Swadling L, Gibbons JM, Pade C, Jensen MP, Diniz MO, et al. Discordant neutralizing antibody and T cell responses in asymptomatic and mild SARS‐CoV‐2 infection. Sci Immunol. 2020;5. 10.1126/sciimmunol.abf3698
    1. Manisty C, Otter AD, Treibel TA, McKnight Á, Altmann DM, Brooks T, et al. Antibody response to first BNT162b2 dose in previously SARS‐CoV‐2‐infected individuals. Lancet. 2021;397:1057–8.
    1. Reynolds CJ, Pade C, Gibbons JM, Butler DK, Otter AD, Menacho K, et al. Prior SARS‐CoV‐2 infection rescues B and T cell responses to variants after first vaccine dose. Science. 2021:eabh1282. 10.1126/science.abh1282
    1. Lackermair K, William F, Grzanna N, Lehmann E, Fichtner S, Kucher HB, et al. Infection with SARS‐CoV‐2 in primary care health care workers assessed by antibody testing. Fam Pract. 2021;38(2):76–9. 10.1093/fampra/cmaa078
    1. Nguyen LH, Drew DA, Graham MS, Joshi AD, Guo C‐G, Ma W, et al. Risk of COVID‐19 among front‐line health‐care workers and the general community: a prospective cohort study. Lancet Public Health. 2020;5:e475–83.
    1. Khalil A, Hill R, Ladhani S, Pattisson K, O’Brien P. COVID‐19 screening of health‐care workers in a London maternity hospital. Lancet Infect Dis. 2021;21:23–4.
    1. Barrett ES, Horton DB, Roy J, Gennaro ML, Brooks A, Tischfield J, et al. Prevalence of SARS‐CoV‐2 infection in previously undiagnosed health care workers at the onset of the U.S. COVID‐19 epidemic. BMC Infect Dis. 2020. Nov 16;20(1):853. 10.1186/s12879-020-05587-2
    1. Peng Y, Felce SL, Dong D, Penkava F, Mentzer AJ, Yao X, et al. An immunodominant NP105–113‐B*07:02 cytotoxic T cell response controls viral replication and is associated with less severe COVID‐19 disease. Nat Immunol. 2022;23(1):50–61. 10.1038/s41590-021-01084-z
    1. Beavis KG, Matushek SM, Abeleda APF, Bethel C, Hunt C, Gillen S, et al. Evaluation of the EUROIMMUN anti‐SARS‐CoV‐2 ELISA assay for detection of IgA and IgG antibodies. J Clin Virol. 2020;129:104468.
    1. Haselmann V, Kittel M, Gerhards C, Thiaucourt M, Eichner R, Costina V, et al. Comparison of test performance of commercial anti‐SARS‐CoV‐2 immunoassays in serum and plasma samples. Clin Chim Acta: Int J Clin Chem. 2020;510:73–8.
    1. Menni C, Valdes AM, Freidin MB, Sudre CH, Nguyen LH, Drew DA, et al. Real‐time tracking of self‐reported symptoms to predict potential COVID‐19. Nat Med. 2020;26:1037–40.
    1. Chang CC, Chow CC, Tellier LCAM, Vattikuti S, Purcell SM, Lee JJ. Second‐generation PLINK: rising to the challenge of larger and richer datasets. GigaScience. 2015;4. 10.1186/s13742-015-0047-8
    1. Zheng X, Shen J, Cox C, Wakefield JC, Ehm MG, Nelson MR, et al. HIBAG—HLA genotype imputation with attribute bagging. Pharmacogenomics J. 2014;14:192–200.
    1. Krammer F, Srivastava K, Alshammary H, Amoako AA, Awawda MH, Beach KF, et al. Antibody responses in seropositive persons after a single dose of SARS‐CoV‐2 mRNA vaccine. N Engl J Med. 2021;384:1372–74.
    1. Goel RR, Apostilidis SA, Painter MM, Matthew D, Pattekar A, Kuthuru O, et al. Distinct antibody and memory B cell responses in SARS‐CoV‐2 naïve and recovered individuals following mRNA vaccination. Sci Immunol. 2021;6(58):eabi6950.
    1. Thursz MR, Kwiatkowski D, Allsopp CE, Greenwood BM, Thomas HC, Hill AV. Association between an MHC class II allele and clearance of hepatitis B virus in the Gambia. N Engl J Med. 1995. Apr 20;332:1065–9. 10.1056/NEJM199504203321604
    1. Smith KJ, Pyrdol J, Gauthier L, Wiley DC, Wucherpfennig KW, et al. Crystal structure of HLA‐DR2 (DRA*0101, DRB1*1501) complexed with a peptide from human myelin basic protein. J Exp Med. 1998;188:1511–20.
    1. Verreck FAW, van de Poel A, Drijfhout JW, Amons R, Coligan JE, Koning F, et al. Natural peptides isolated from Gly86/Val86‐containing variants of HLA‐DR1, ‐DR11, ‐DR13, and ‐DR52. Immunogenetics. 1996;43:392–7.
    1. Davenport MP, Quinn CL, Chicz RM, Green BN, Willis AC, Lane WS, et al. Naturally processed peptides from two disease‐resistance‐associated HLA‐ DR13 alleles show related sequence motifs and the effects of the dimorphism at position 86 of the HLA‐DR beta chain. Proc Natl Acad Sci U S A. 1995;92:6567–71.
    1. Newton‐Nash DK, Eckels DD. Differential effect of polymorphism at HLA‐DR1 beta‐chain positions 85 and 86 on binding and recognition of DR1‐restricted antigenic peptides. J Immunol. 1993;150:1813–21.
    1. Ong B, Willcox N, Wordsworth P, Beeson D, Vincent A, Altmann D, et al. Critical role for the Val/Gly86 HLA‐DR beta dimorphism in autoantigen presentation to human T cells. Proc Natl Acad Sci U S A. 1991;88:7343–7.

Source: PubMed

3
Prenumerera