Chattopadhyay C, Natvig J B, Chattopadhyay H
Scand J Immunol. 1980;11(4):455-9. doi: 10.1111/j.1365-3083.1980.tb00013.x.
Patient K.L. with X-linked hypogammaglobulinaemia showed excessive suppressor T-cell activity both in the lymphocytes from the rheumatoid synovial tissue and in the peripheral blood lymphocyte compartment. This was in marked contrast to the findings in the lymphocytes from synovial tissue of patients with classical rheumatoid arthritis (RA), which were clearly deficient in suppressor T-cell activity. These findings further support the existence of distinctly different pathogenetic mechanisms in the two types of rheumatoid inflammation. It also demonstrates that patients with X-linked hypogammaglobulinaemia may have excessive suppressor T-cell activity not only in their peripheral blood lymphocytes but also in local chronic inflammatory tissue such as the rheumatoid joint inflammation.
患有X连锁低丙种球蛋白血症的患者K.L.在类风湿性滑膜组织淋巴细胞和外周血淋巴细胞区室中均表现出过度的抑制性T细胞活性。这与经典类风湿性关节炎(RA)患者滑膜组织淋巴细胞的研究结果形成鲜明对比,后者的抑制性T细胞活性明显不足。这些发现进一步支持了两种类风湿性炎症存在明显不同的发病机制。这也表明,患有X连锁低丙种球蛋白血症的患者不仅在外周血淋巴细胞中,而且在局部慢性炎症组织如类风湿性关节炎症中可能具有过度的抑制性T细胞活性。