Kuipers J G, Jacobs R, Kemper A, Zeidler H, Schmidt R E
Department of Clinical Immunology, Hannover Medical School, Germany.
Rheumatol Int. 1994;14(4):163-8. doi: 10.1007/BF00579702.
The T gamma-lymphoproliferative syndrome is characterized by a proliferation of large granular lymphocytes (LGL). It is often associated with neutropenia, and in 30% of cases with rheumatoid arthritis (RA). Phenotypic analysis has demonstrated that in most cases of RA with T gamma-proliferative disease, the LGL represent T cells with a clonal rearrangement of the alpha/beta T cell receptor (TCR2). Here, three patients with gamma/delta TCR1+ LGL proliferation suffering from long-standing arthritis and neutropenia are described. The first patient with RA showed an expansion of a heterogeneous CD2+ CD16+ CD56- LGL population, of which 30% coexpressed TCR1 with V delta 1 rearrangement. The second patient with ankylosing spondylitis and RA was suffering from proliferation of TCR1+ (V gamma 9-, V delta 1-), CD2+ CD16- CD56- LGL with low coexpression of CD8. The third patient with RA was suffering from a proliferation of TCR1+ (V delta 1+, V gamma 9-) CD4- CD8- CD16- CD56- lymphocytes. On the basis of these unusual findings, the pathogenetic role of TCR1+ T cells in RA is discussed.
Tγ淋巴细胞增殖综合征的特征是大颗粒淋巴细胞(LGL)增殖。它常与中性粒细胞减少相关,在30%的病例中与类风湿关节炎(RA)相关。表型分析表明,在大多数伴有Tγ增殖性疾病的RA病例中,LGL代表具有α/βT细胞受体(TCR2)克隆重排的T细胞。本文描述了3例患有γ/δTCR1+LGL增殖、长期关节炎和中性粒细胞减少的患者。首例RA患者显示异质性CD2+CD16+CD56-LGL群体扩增,其中30%共表达TCR1且Vδ1重排。第二例患有强直性脊柱炎和RA的患者,其TCR1+(Vγ9-,Vδ1-)、CD2+CD16-CD56-LGL增殖,CD8共表达率低。第三例RA患者,其TCR1+(Vδ1+,Vγ9-)CD4-CD8-CD16-CD56-淋巴细胞增殖。基于这些不寻常的发现,讨论了TCR1+T细胞在RA中的致病作用。