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Characterization of MHC class I alleles in sooty mangabeys as a tool for evaluating cellular immunity in natural hosts of SIV infection

Authors :
Benjamin J. Metcalf
Melissa Kasheta
Caitlin Kasala-Hallinan
Dollnovan Tran
Amitinder Kaur
David H. O’Connor
Cristian Apetrei
Julie A. Karl
Zichun Wang
R. Paul Johnson
James G. Else
Source :
Immunogenetics. 67:447-461
Publication Year :
2015
Publisher :
Springer Science and Business Media LLC, 2015.

Abstract

Although immune pressure exerted by MHC class I-restricted cytotoxic T lymphocytes (CTL) are an important determinant of outcome in pathogenic HIV and SIV infection, lack of data on MHC class I genes has hampered study of its role in natural hosts with nonpathogenic SIV infection. In this study we cloned and characterized full-length MHC class I genes derived from the cDNA library of two unrelated naturally-infected sooty mangabeys (Cercocebus atys) in whom SIV-specific CTL epitopes were previously mapped. Twenty one full-length MHC Class I alleles consisting of five MHC-A (Ceat-A), 13 MHC-B (Ceat-B), and three MHC-E (Ceat-E) alleles were identified. Sequence-specific primers (SSP) for high throughput screening of genomic DNA by PCR were developed for 16 of the 18 Ceat-A and Ceat-B alleles. Screening of 62 SIV-negative and 123 SIV-infected sooty mangabeys at the Yerkes National Primate Research Center (YNPRC) revealed the presence of up to four MHC-A and eight MHC-B alleles in individual mangabeys, indicating that similar to macaque species, mangabeys have at least two duplications of the MHC-A locus, and four duplications of the MHC-B locus in the absence of an MHC-C locus. Using stable transfectants of Ceat MHC Class I alleles in the MHC-null 721.221 cell line, we identified Ceat-B*12:01 as the restricting allele of a previously reported Nef20–28 CTL epitope. Ceat-B*1201/Nef20–28 tetramers identified tetramer-positive CD8+ T lymphocytes in Ceat-B*1201-positive SIV-infected mangabeys. This study has laid the groundwork for comprehensive analysis of CTL and SIV evolution in a natural host of SIV infection.

Details

ISSN :
14321211 and 00937711
Volume :
67
Database :
OpenAIRE
Journal :
Immunogenetics
Accession number :
edsair.doi.dedup.....2e5c1f79aa95209815ddfd2e68de4cb2
Full Text :
https://doi.org/10.1007/s00251-015-0853-2