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The role of HLA genotypes in understanding the pathogenesis of severe COVID-19
Fatemeh Arab1, Samaneh Mollazadeh2, Farnaz Ghayourbabaei3
1Medical Genetics and Molecular Medicine Department, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Insights
Human leukocyte antigen (HLA) profiles influence COVID-19 severity. Genetic variations in HLA class I may lead to insufficient immune activation, increasing susceptibility to severe coronavirus disease 2019 (COVID-19).
Area of Science:
- Immunogenetics
- Virology
- Genomics
Background:
- The COVID-19 pandemic, caused by SARS-CoV-2, presents varied severity among individuals, with underlying genetic factors still under investigation.
- Host genetic factors, particularly variations in immune system genes like human leukocyte antigen (HLA) profiles, are crucial in determining the body's response to viral infections.
- The innate and adaptive immune systems, with HLA playing a key role in the latter, are central to combating viral pathogens like SARS-CoV-2.
Purpose of the Study:
- To investigate the association between human leukocyte antigen (HLA) allelic diversity and susceptibility to severe COVID-19.
- To explore how variations in HLA class I genotypes might impact immune system activation and the body's response to SARS-CoV-2 infection.
- To identify potential genetic predictors of COVID-19 severity for improved preventive and therapeutic strategies.
Main Methods:
- Comparative analysis of HLA allelic diversity between COVID-19 infected individuals and uninfected individuals of the same race.
- Focus on HLA class I genotypes and their role in antigen presentation to T lymphocytes.
- Assessment of immune response, including cytokine secretion (e.g., interferons), in relation to HLA profiles.
Main Results:
- Specific HLA class I genotypes may be associated with insufficient immune system activation upon SARS-CoV-2 exposure.
- Inadequate binding of viral antigens by certain HLA class I molecules can lead to impaired T lymphocyte recognition and activation.
- This insufficient immune response may result in delayed or absent secretion of crucial antiviral cytokines like interferons.
Conclusions:
- HLA-I genetic variations are significant host factors influencing COVID-19 disease progression and severity.
- Understanding HLA diversity can help identify individuals at higher risk for severe COVID-19.
- This knowledge aids in developing targeted preventive measures and therapeutic interventions for coronavirus disease 2019.
Abstract:
The coronavirus disease 2019 (COVID-19) pandemic has caused human tragedy through the global spread of the viral pathogen SARS-CoV-2. Although the underlying factors for the severity of COVID-19 in different people are still unknown, several gene variants can be used as predictors of disease severity, particularly variations in viral receptor genes such as angiotensin-converting enzyme 2 (ACE2) or major histocompatibility complex (MHC) genes. The reaction of the immune system, as the most important defense strategy in the case of viruses, plays a decisive role. The innate immune system is important both as a primary line of defense and as a trigger of the acquired immune response. The HLA-mediated acquired immune response is linked to the acquired immune system. In various diseases, it has been shown that genetic alterations in components of the immune system can play a crucial role in how the body responds to pathogens, especially viruses. One of the most important host genetic factors is the human leukocyte antigen (HLA) profile, which includes HLA classes I and II and may be symbolic of the diversity of immune response and genetic predisposition in disease progression. COVID-19 will have direct contact with the acquired immune system as an intracellular pathogen after exposure to the proteasome and its components through class I HLA. Therefore, it is assumed that in different genotypes of the HLA-I class, an undesirable supply causes an insufficient activation of the immune system. Insufficient binding of antigen delivered by class I HLA to host lymphocytes results in uncertain identification and insufficient activation of the acquired immune system. The absence of secretion of immune cytokines such as interferons, which play an important role in controlling viral infection in the early stages, is a complication of this event. Understanding the allelic diversity of HLA in people infected with coronavirus compared with uninfected people of one race not only allows identification of people with HLA susceptible to COVID-19 but also provides better insight into the behavior of the virus, which helps to take effective preventive and curative measures earlier.
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