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腺苷脱氨酶缺陷型重症联合免疫缺陷中通过外周血白细胞进行免疫重建。

Immunoreconstitution by peripheral blood leukocytes in adenosine deaminase-deficient severe combined immunodeficiency.

作者信息

Rich K C, Richman C M, Mejias E, Daddona P

出版信息

J Clin Invest. 1980 Aug;66(2):389-95. doi: 10.1172/JCI109868.

Abstract

Transplantation of histocompatible allogeneic peripheral blood leukocytes resulted in successful reconstitution of an adenosine deaminase (ADA)-deficient, severe combined immune-deficient patient. Erythrocyte transfusions before the transplant were associated with a rise of serum immunoglobulin concentration to normal without improvement in T cell function. The patient received 5 x 10(7) peripheral blood mononuclear leukocytes/kg obtained from the histocompatible father by leukopheresis. 3 wk after the transplant the lymphocyte count, proportion of E rosetting lymphocytes, and the ADA content of the patient's mononuclear leukocytes became normal while the phytohemagglutinin-stimulated blastogenic responses improved and became normal 52 d after the transplant. Antibody response to diphtheria immunization and response to naturally acquired herpes simplex infection were normal while isohemagglutinins progressively increased. Immunization with a neoantigen, bacteriophage phiX 174, resulted in a small but definite antibody response but no amplification of the response after secondary immunization. A positive reaction to a skin test for Candida albicans developed. Erythrocyte deoxy ATP (dATP) concentration decreased during the course of erythrocyte transfusions. 9 mo after the transplant, the erythrocyte dATP was elevated to twice pretransfusion levels while mononuclear leukocyte dATP varied from normal to elevated during the first 4 mo of the posttransplant period, but remained normal during the last 8 mo. The improvement in immune function persisted during the 12-mo posttransplant observation period while the mononuclear leukocyte ADA concentration stabilized at approximately 0.25 of normal, which is similar to the enzyme activity of the donor cells. This in vivo study supports the hypothesis that lymphoid precursor cells are present in peripheral blood which may partially reconstitute an immune-deficient recipient.

摘要

移植组织相容性同种异体外周血白细胞成功重建了一名腺苷脱氨酶(ADA)缺陷的重症联合免疫缺陷患者的免疫系统。移植前的红细胞输血使血清免疫球蛋白浓度升至正常水平,但T细胞功能并未改善。该患者接受了通过白细胞分离术从组织相容性父亲处获得的5×10⁷外周血单个核白细胞/kg。移植后3周,患者的淋巴细胞计数、E花环形成淋巴细胞比例以及单个核白细胞的ADA含量恢复正常,而植物血凝素刺激的母细胞化反应有所改善,并在移植后52天恢复正常。对白喉免疫的抗体反应以及对自然获得的单纯疱疹感染的反应正常,而异血凝素逐渐增加。用新抗原噬菌体φX 174免疫产生了微弱但明确的抗体反应,但二次免疫后反应未增强。对白色念珠菌皮肤试验出现阳性反应。在红细胞输血过程中,红细胞脱氧ATP(dATP)浓度降低。移植后9个月,红细胞dATP升高至输血前水平的两倍,而单个核白细胞dATP在移植后的前4个月从正常变化至升高,但在最后8个月保持正常。在移植后12个月的观察期内,免疫功能持续改善,而单个核白细胞ADA浓度稳定在正常水平的约0.25,这与供体细胞的酶活性相似。这项体内研究支持了外周血中存在淋巴前体细胞的假说,这些细胞可能部分重建免疫缺陷受体的免疫系统。

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