Publication:
Major Histocompatibility Complex Class I Chain-Related α (MICA) STR Polymorphisms in COVID-19 Patients.

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Date

2022-06-22

Authors

Gutierrez-Bautista, Juan Francisco
Martinez-Chamorro, Alba
Rodriguez-Nicolas, Antonio
Rosales-Castillo, Antonio
Jimenez, Pilar
Anderson, Per
Lopez-Ruz, Miguel Angel
Lopez-Nevot, Miguel Angel
Ruiz-Cabello, Francisco

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MDPI AG
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Abstract

The SARS-CoV-2 disease presents different phenotypes of severity. Comorbidities, age, and being overweight are well established risk factors for severe disease. However, innate immunity plays a key role in the early control of viral infections and may condition the gravity of COVID-19. Natural Killer (NK) cells are part of innate immunity and are important in the control of virus infection by killing infected cells and participating in the development of adaptive immunity. Therefore, we studied the short tandem repeat (STR) transmembrane polymorphisms of the major histocompatibility complex class I chain-related A (MICA), an NKG2D ligand that induces activation of NK cells, among other cells. We compared the alleles and genotypes of MICA in COVID-19 patients versus healthy controls and analyzed their relation to disease severity. Our results indicate that the MICA*A9 allele is related to infection as well as to symptomatic disease but not to severe disease. The MICA*A9 allele may be a risk factor for SARS-CoV-2 infection and symptomatic disease.

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MeSH Terms

COVID-19
Histocompatibility Antigens Class I
Humans
Major Histocompatibility Complex
Polymorphism, Genetic
SARS-CoV-2

DeCS Terms

Antígenos de histocompatibilidad Clase I
Complejo mayor de histocompatibilidad
Polimorfismo genético
SARS-CoV-2

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Keywords

MICA, MICA STR polymorphisms, NK cells, SARS-CoV-2, innate immunity

Citation

Gutiérrez-Bautista JF, Martinez-Chamorro A, Rodriguez-Nicolas A, Rosales-Castillo A, Jiménez P, Anderson P, et al. Major Histocompatibility Complex Class I Chain-Related α (MICA) STR Polymorphisms in COVID-19 Patients. Int J Mol Sci. 2022 Jun 23;23(13):6979.