Analysis of Gag-specific cytotoxic T lymphocytes in simian immunodeficiency virus-infected rhesus monkeys by cell staining with a tetrameric major histocompatibility complex class I peptide complex

被引:247
作者
Kuroda, MJ
Schmitz, JE
Barouch, DH
Craiu, A
Allen, TM
Sette, A
Watkins, DI
Forman, MA
Letvin, NL
机构
[1] Harvard Univ, Sch Med, Div Viral Pathogenesis, Dept Med,Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[2] Univ Wisconsin, Wisconsin Reg Primate Res Ctr, Madison, WI 53715 USA
[3] Univ Wisconsin, Dept Pathol & Lab Med, Madison, WI 53715 USA
[4] Coulter Corp, Miami, FL 33116 USA
[5] Eppimune, San Diego, CA 92121 USA
关键词
D O I
10.1084/jem.187.9.1373
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A tetrameric recombinant major histocompatibility complex (MHC) class I-peptide complex was used as a staining reagent in flow cytometric analyses to quantitate and define the phenotype of Gag-specific cytotoxic T lymphocytes (CTLs) in the peripheral blood of simian immunodeficiency virus macaque (SIVmac)-infected rhesus monkeys. The heavy chain of the rhesus monkey MHC class I molecule Mamu-A*01 and beta(2)-microglobulin were refolded in the presence of an SIVmac Gag synthetic peptide (p11C, C-M) representing the optimal nine-amino acid peptide of Mamu-A*01-restricted predominant CTL epitope to create a tetrameric Mamu-A*01/p11C, C-M complex. Tetrameric Mamu-A*01/p11C, C-M complex bound to T cells of SIVmac-infected, Mamu-A*01(+), but not uninfected, Mamu-A*01(+), or infected, Mamu-A*01(-) rhesus monkeys. Specific staining of peripheral blood mononuclear cells (PBMC) from SIVmac-infected, Mamu-A*01(+) rhesus monkeys was only found in the cluster of differentiation (CD)8 alpha/beta(+) T lymphocyte subset and the percentage of CD8 alpha/beta(+) T cells in the peripheral blood of four SIVmac-infected, Mamu-A*01(+) rhesus monkeys staining with this complex ranged hom 0.7 to 10.3%. Importantly, functional SIVmac Gag p11C-specific CTL activity was seen in sorted and expanded tetrameric Mamu-A*01/p11C, C-M complex-binding, but not nonbinding, CD8 alpha/beta(+) T cells. Furthermore, the percentage of CD8 alpha/beta(+) T cells binding this tetrameric Mamu-A*01/p11C, C-M complex correlated well with p11C-specific cytotoxic activity as measured in both bulk and limiting dilution effector frequency assays. Finally, phenotypic characterization of the cells binding this tetrameric complex indicated that this lymphocyte population is heterogeneous. These studies indicate the power of this approach for examining virus-specific CTLs in in vivo settings.
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页码:1373 / 1381
页数:9
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