Journal of Southern Medical University ›› 2006, Vol. 26 ›› Issue (08): 1128-1131.

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Complementarity-determining region 3 analysis of T cell receptor beta chain variable region in peripheral blood mononuclear cells of patients with systemic lupus erythematosus

LUO Wei1, MA Li1, YAO Xin-sheng1, ZOU Hong-yun1, WEN Qian1, RUAN Guang-ping1, WANG Xiao-ning2 1Institute of Molecular Immunology, School of Biotechnology, Southern Medical University, Guangzhou 510515, China; 2School of Bioscience and Bioengineering, Southon China University of Technology, Guangzhou 510641, China   

  1. 南方医科大学生物技术学院分子免疫学研究所; 华南理工大学生物科学与工程学院 广东广州510515; 广东广州510515; 广东广州510641;
  • Online:2006-08-20 Published:2006-08-20

Abstract: Objective To analyze the drift of the complementarity-determining region 3 (CDR3) of T cell receptor (TCR) beta chain variable region (TCR BV) in peripheral blood mononuclear cells (PBMCs) of patients with systemic lupus erythematosus. Methods Immunoscope spectratyping techniques was used to analyze the distribution of TCRβ chain CDR3 in 5 normal blood donors and the dominant CDR3 in the PBMCs in 5 SLE patients. Sequence analysis of the CDR3 region in monoclonal or oligoclonal T cells was performed. Results The spectratypes of TCR BV gene CDR3 region showed Gaussian distribution in the 5 normal blood donors. The 5 SLE patients, however, displayed anomalous proliferation and oligoclonal expansion of the T cells was observed in different TCR BV families with different CDR3 sequences. Conclusion Noticeable drift of TCRβ chain CDR3 can be seen in active SLE, indicating possible association of selective expression of TCR with immune pathogenesis in SLE. Determination of specific TCR CDR3 sequence provides a new means for studying the pathogenesis and personalized treatment of SLE. 

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