Defect of lck in a patient with common variable immunodeficiency.

T. Sawabe, T. Horiuchi, M. Nakamura, H. Tsukamoto, K. Nakahara, S. I. Harashima, T. Tsuchiya, S. Nakano

研究成果: Contribution to journalArticle査読

27 被引用数 (Scopus)

抄録

Common variable immunodeficiency (CVID) is a congenital immunological disorder characterized by defective antibody production with normal count of peripheral B lymphocytes. The basic immunologic defects that leads to CVID are still unknown, however, a proportion of CVID is suggested to be caused by decreased CD4+ helper T cell activity. In addition, recent reports indicate that a defect of T cell receptor (TCR)-associated signaling molecules results in congenital immune deficiency in human. In the present study, we investigated lck, a signaling molecule downstream of TCR, in a patient with CVID plus CD4 lymphopenia, and found an aberrantly spliced lck transcript lacking the entire exon 7 associated with the decrease in the expression of lck protein. An identical splicing abnormality has been previously demonstrated in a case of severe combined immunodeficiency with selective CD4 lymphopenia, although the case showed almost complete loss of the expression of lck protein. Considering these findings, the aberrant splicing of lck gene is suggested to be correlated, at least with a subset of congenital immunodeficiency plus CD4 lymphopenia.

本文言語英語
ページ(範囲)609-614
ページ数6
ジャーナルInternational journal of molecular medicine
7
6
DOI
出版ステータス出版済み - 6 2001

All Science Journal Classification (ASJC) codes

  • 遺伝学

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