PMID- 21911137 OWN - NLM STAT- MEDLINE DCOM- 20120110 LR - 20110913 IS - 1873-2623 (Electronic) IS - 0041-1345 (Linking) VI - 43 IP - 7 DP - 2011 Sep TI - Monitoring of cytomegalovirus-specific CD8+ T-cell response with major histocompatibility complex pentamers in kidney transplant recipients. PG - 2636-40 LID - 10.1016/j.transproceed.2011.05.051 [doi] AB - INTRODUCTION: Cytomegalovirus (CMV) can reactivate causing serious clinical problems during immunosuppression. CMV-specific CD8(+) T cells play an important role in the control of CMV reactivation. Using pentameric major histocompatibility complex (MHC) peptide complexes, we investigated cellular immune responses to CMV among healthy individuals and kidney transplantation recipients in Korea, which is an endemic area of CMV infection. MATERIALS AND METHODS: Analysis of CMV-specific T cells was performed on 28 healthy individuals and 40 recipients who bore human leukocyte antigen (HLA)-A2 or -A24. CMV pp65 pentamer-binding cells incubated with various monoclonal antibodies were measured by four-color flow cytometry. RESULTS: Detectable levels of pentamer(+) CD8(+) T cells were present in 109/139 samples (78.4%) that stained with the A*02NLV-pentamer, while 15/67 samples (22.4%) stained with the A*24QYD-pentamer (P < .01). Among patients with HLA-A2, 22/24 (91.7%) samples showing positive CMV antigenemia revealed detectable pentamer(+) CD8(+) T cells, while 87/115 (75.7%) displaying negative CMV antigenemia had detectable pentamer(+) CD8(+) T cells (P = .04). There was no significant difference in percentages of pentamer(+) CD8(+) T cells between patients who did versus who did not experience episodes of CMV infection. The subpopulation of CMV-specific CD8(+) T cells in transplantation recipients was evaluated using phenotypic markers; memory cells comprised the majority of the CMV-specific CD8(+) T-cell population. CONCLUSION: The A*02NLV-pentamer complex was useful to monitor CMV-specific T cells. However, MHC pentamer-based techniques did not provide a clear distinction between patients who are or are not at risk for CMV infection. CI - Copyright (c) 2011 Elsevier Inc. All rights reserved. FAU - Lee, S AU - Lee S AD - Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. FAU - Park, J B AU - Park JB FAU - Kim, E Y AU - Kim EY FAU - Joo, S Y AU - Joo SY FAU - Shin, E C AU - Shin EC FAU - Kwon, C H AU - Kwon CH FAU - Joh, J W AU - Joh JW FAU - Kim, S J AU - Kim SJ LA - eng PT - Journal Article PL - United States TA - Transplant Proc JT - Transplantation proceedings JID - 0243532 SB - IM MH - Adult MH - CD8-Positive T-Lymphocytes/*immunology MH - Case-Control Studies MH - Cytomegalovirus/*immunology MH - Female MH - Flow Cytometry MH - Fluorescent Antibody Technique MH - Humans MH - *Kidney Transplantation MH - *Major Histocompatibility Complex MH - Male MH - Middle Aged MH - Monitoring, Physiologic EDAT- 2011/09/14 06:00 MHDA- 2012/01/11 06:00 CRDT- 2011/09/14 06:00 PHST- 2011/04/21 00:00 [received] PHST- 2011/05/09 00:00 [accepted] PHST- 2011/09/14 06:00 [entrez] PHST- 2011/09/14 06:00 [pubmed] PHST- 2012/01/11 06:00 [medline] AID - S0041-1345(11)00866-9 [pii] AID - 10.1016/j.transproceed.2011.05.051 [doi] PST - ppublish SO - Transplant Proc. 2011 Sep;43(7):2636-40. doi: 10.1016/j.transproceed.2011.05.051.