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Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Vaccine 2021 ; 39 (15): 2110-2116 Nephropedia Template TP
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Assessment of SARS-CoV-2 specific CD4(+) and CD8 (+) T cell responses using MHC class I and II tetramers #MMPMID33744048
Poluektov Y; George M; Daftarian P; Delcommenne MC
Vaccine 2021[Apr]; 39 (15): 2110-2116 PMID33744048show ga
The success of SARS-CoV-2 (CoV-2) vaccines is measured by their ability to mount immune memory responses that are long-lasting. To achieve this goal, it is important to identify surrogates of immune protection, namely, CoV-2 MHC Class I and II immunodominant pieces/epitopes and methodologies to measure them. Here, we present results of flow cytometry-based MHC Class I and II QuickSwitch(TM) platforms for assessing SARS-CoV-2 peptide binding affinities to various human alleles as well as the H-2 Kb mouse allele. Multiple SARS-CoV-2 potential MHC binders were screened and validated by QuickSwitch testing. The screen included 31 MHC Class I and 19 MHC Class II peptides predicted to be good binders by the IEDB web resource provided by NIAID. While several predicted peptides with acceptable theoretical Kd showed poor MHC occupancies, fourteen MHC class II and three MHC class I peptides showed promiscuity in that they bind to multiple MHC molecule types. In addition to providing important data towards the study of the SARS-CoV-2 virus and its presented antigenic epitopes, the peptides identified in this study can be used in the QuickSwitch platform to generate MHC tetramers. With those tetramers, scientists can assess CD4 + and CD8 + immune responses to these different MHC/peptide complexes.
|Animals[MESH]
|CD4-Positive T-Lymphocytes/*immunology[MESH]
|CD8-Positive T-Lymphocytes/*immunology[MESH]
|COVID-19/*immunology[MESH]
|Epitopes, T-Lymphocyte/immunology[MESH]
|Histocompatibility Antigens Class I/*immunology[MESH]
|Histocompatibility Antigens Class II/*immunology[MESH]