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Commentary: COVID-19 and the Path to Immunity James LM, Tsilibary EP, Charonis S, Georgopoulos AP. Commentary: COVID-19 and the Path to Immunity. J Immunological Sci. (2020); 4(4): 31-33 Journal of Immunological Sciences Commentary Open Access Commentary: COVID-19 and the Path to Immunity Lisa M. James1,2,3,4; Effie-Photini C. Tsilibary1,2; Spyros Charonis1,2; Apostolos P. Georgopoulos1,2,3,4* 1Brain Sciences Center, Department of Veterans Affairs Health Care System, Minneapolis, MN, USA 2Department of Neuroscience, University of Minnesota Medical School, Minneapolis, MN, USA 3Department of Psychiatry, University of Minnesota Medical School, Minneapolis, MN, USA 4Center for Cognitive Sciences, University of Minnesota, Minneapolis, MN, USA Introduction Article Info A recently published Viewpoint1 underscored the importance Article Notes Received: November 18, 2020 of T- and B- cell-mediated immune responses to severe acute Accepted: November 23, 2020 respiratory syndrome coronavirus 2 (SARS-CoV-2) but omitted to *Correspondence: *Dr. Apostolos P. Georgopoulos, Brain Sciences Center, Department of Veterans Affairs Health Care System, mention the very first step necessary to trigger those responses, Minneapolis, MN 55417, USA; Email: [email protected]. namely the formation of a complex between the virus antigen and © 2020 Georgopoulos AP. This article is distributed under the a suitably matching Human Leukocyte Antigen (HLA) molecule. terms of the Creative Commons Attribution 4.0 International Here, we discuss the role of HLA in individual variability in immune License. response to SARS-CoV-2, emphasizing the implications of HLA as potentially underlying sustained symptoms seen in “long-COVID”, as distinguished from the severe, acute COVID-19, which is associated withLong-COVID “stormy” immune response. Increasing evidence documents sustained health effects of SARS-CoV-2, the virus responsible for the ongoing coronavirus-19 been(COVID-19) reported pandemic, in patients in upa subset to two of months infected after individuals. onset of symptoms Symptoms including persistent fatigue, dyspnea, joint4 pain, and chest pain have2,3 as have anecdotal reports of “brain fog” ; however, scientific study of “long COVID” is just beginning and the reasons underlying symptom persistence, even among those who experienced mild cases of SARS-CoV-2COVID-19, are infection not yet understood. Current hypotheses regarding7 the cause of long-COVID5,6 include organ damage resulting from acute and extensive and excessive inflammation . furtherNotably, explorationinadequate ofability the interactionto develop neutralizingbetween SARS-CoV-2 antibodies virus has andalso hostbeen immuneobserved response in some8 COVID patients, leading to a call for . Human leukocyte antigen (HLA), a key player in immune system responses to viral and other foreign antigens, has been9-11 implicated in the variability in severity of acute cases of COVID-19 . We contend that HLA makeup likely also plays a role in sustained symptoms observed in long-COVID and is highly relevantHLA plays to COVID-19 a critical prevention role in immunity and intervention. Due to selective pressure and co-evolution with pathogens, HLA is the most polymorphic region of the human genome, resulting in relatedsubstantial illnesses individual and has variability been implicated in cell-surface in treatment HLA molecules. of infectious This diseasesvariability, and which in hasvaccine been responsivenessshown to impact12 the course of pathogen- , results in differential Page 31 of 33 James LM, Tsilibary EP, Charonis S, Georgopoulos AP. Commentary: COVID-19 and the Journal of Immunological Sciences Path to Immunity. J Immunological Sci. (2020); 4(4): 31-33 in an binding affinity of HLA molecules with foreign antigens. For example, administration of a vaccine may not result mediatedThe formation immune of a responsescomplex between that are a critical foreign to antigen successful and tibody production and immunological memory, the a suitably matched HLA molecule facilitates T- and B-cell very goal of vaccination, in those without suitable HLA makeup – i.e., in the absence of HLA that sufficiently host protection. Specifically, the HLA-antigen complex is thebind serum with vaccineof individuals antigens. affected Indeed, with in individualschronic conditions lacking exported to the cell surface where it is presented to CD8+ decadesspecific HLA,after vaccine-derivedvaccination14 antigens have been found in cytotoxic T-cells which kill infected cells and CD4+ T-cells to initiate the formation of antibodies by B-cells, resulting . It stands to reason that HLA is in adaptive immunity. However, when this process fails, likely to similarly play a role in vaccine response aimed at e.g. because of lack of appropriate HLA makeup, immune prevention of COVID-19. That is, a small subset of individuals whichresponses could are not deficient be eliminated resulting in chronic disease due to who lack HLA composition that permits successful binding the persistence of offending antigens13 or viral pathogens to the SARS-CoV-2 antigen and stimulation of an immune Long-COVID and persistent .antigens response are unlikely to benefit from vaccination. Similarly, HLA reflects an important consideration with regard to effective treatment of COVID-19, particularly among the Since HLA variations affect antigen binding affinity, long-haulers. Since those with sustained symptoms are and, consequently, contribute to variability in B- and T-cell presumably unable to mount a sufficient immune response mediated immune response to pathogens, individual to eliminate the virus, immunotherapy aimed directly at variability in HLA could account for the differences in the elimination of the antigens (e.g, via monoclonalned symptoms or polyclonal in magnitude of antibody and T-cell response and the wide antibodies) represents a promising treatment 14avenue for range of clinical disease severity observed with COVID-19, the subset of COVID-19 cases with sustai in otherwise immunocompetent individuals. Indeed, it particular,Conclusion as demonstrated in other conditions . was found that variability in the regional distribution of the two most frequent HLA haplotypes in Italy overlapped variability in disease course and chronicity as well as in inwith silico the variabilityanalyses havein COVID-19 demonstrated incidence allelic9 and variationsmortality Taken together, HLA is likely implicated in individual observed in Northern vs Southern Italy . Furthermore, 10,11 prevention and intervention effectiveness. The blind spot in SARS-CoV-2 binding affinity . While those studies created in the field by lack of consideration of variation support associations between HLA and acute COVID-19 in HLA with respect to binding affinity of SARS-CoV-2 will researchseverity, inwe other are diseasesnot aware has ofindeed any providedstudy definitively evidence hamper efforts at forecasting disease outcomes, developing linking long-COVID to specific HLA genotypes. However, effective interventions, and creating durable protection. Rather, identification11 of specific epitopes in the SARS- of sustained antigen persistence and chronic symptoms13,14 CoV-2 spike glycoprotein that bind with high affinity to HLA in individuals lacking specific “protective” HLA . That Class II alleles would prove valuable in understanding is, it has been shown that “protective” HLA suitably bind adaptive immunity to COVID-19 and advancing successful with and eliminate antigens, protecting against chronic interventions by developing vaccines based on such HLA- disease whereas the absence of protective HLA contribute relatedFunding SARS-CoV-2 epitopes. to immune-mediated disease. Based on those findings, we suspect that the absence of a sufficient HLA-SARS- by the University of Minnesota (the Anita Kunin Chair in CoV-2 antigen match leads to the persistence of SARS viral Partial funding for this Commentary was provided antigens, thereby contributing to sustained symptoms observed in “long-haulers”, a hypothesis that remains to be Women’s Healthy Brain Aging, the Brain and Genomics investigated.Consideration of HLA in COVID prevention and Fund, the McKnight Presidential Chair of Cognitive intervention Neuroscience, and the American Legion Brain Sciences Chair) and the Minneapolis Veterans Affairs Healthcare System. The sponsors had no role in the current study and promoteNumerous recovery; alleles areresearch likely in to our bind lab withis currently SARS- design, analysis or interpretation, or in the writing of this CoV-2 antigens to facilitate elimination of viral antigens paper. The contents do not represent the views of the U.S. Department of Veterans Affairs or the United States underway to identify SARS-CoV-2-protective HLA alleles as Government.Author contributions such findings bear implications for SARS-CoV-2 prevention and treatment. With regard to other infectious diseases it is well-established that HLA variation is implicated in LMJ and APG wrote the manuscript; all contributed to both vaccine responsiveness and treatment response. editing. Page 32 of 33 James LM, Tsilibary EP, Charonis S, Georgopoulos AP. Commentary: COVID-19 and the Journal of Immunological Sciences Path to Immunity. J Immunological Sci. (2020); 4(4): 31-33 Conflicts of Interest The authors declare that the research was conducted in 7. Tay MZ, Poh CM, Rénia L, et al. The trinity of COVID-19: immunity, inflammation, and intervention. Nature Rev Microbiol. 2020; 20: 363- 374. doi: OI: 10.1038/s41577-020-0311-8 the absence of any commercial or financial
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