Nagura H, Kohler P F, Brown W R
Lab Invest. 1979 Jan;40(1):66-73.
The immunoglobulin constituents of hypertrophied lymphoid nodules in the intestinal tracts of six patients with the variable immunodeficiency syndrome and one patient with selective IgA deficiency were evaluated by the peroxidase-labeled antibody technique. The nodules were found to contain a dense population of IgM-bearing lymphocytes and much intercellular IgM. Evidence that the cells were engaged in IgM synthesis was the presence of the immunoglobulin in the perinuclear spaces and endoplasmic reticulum. Most of the IgM lymphocytes also had surface membrane IgM, and both kappa and lambda light chains were found in lymphocytes of individual nodules. Only a few cells containing IgD, IgG, or J chain, and none containing IgA, were found. We conclude that the intestinal lymphoid nodules associated with hypogammaglobulinemic states are populated principally by IgM B-lymphocytes of polyclonal origin.
采用过氧化物酶标记抗体技术,对6例可变免疫缺陷综合征患者和1例选择性IgA缺乏患者肠道内肥大淋巴小结的免疫球蛋白成分进行了评估。发现这些小结含有大量携带IgM的淋巴细胞和大量细胞间IgM。细胞参与IgM合成的证据是在核周间隙和内质网中存在免疫球蛋白。大多数IgM淋巴细胞也有表面膜IgM,并且在单个小结的淋巴细胞中发现了κ链和λ链。仅发现少数含有IgD、IgG或J链的细胞,未发现含有IgA的细胞。我们得出结论,与低丙种球蛋白血症状态相关的肠道淋巴小结主要由多克隆来源的IgM B淋巴细胞构成。