Airò P, Cattaneo R, Franceschini F, Migliosi G, Ferrari C M, Airò R
Cattedra di Immunologia Clinica, Università di Brescia.
Boll Ist Sieroter Milan. 1988;67(4):290-4.
Lymphocytosis of large granular lymphocytes (LGL) has been observed in 6 patients splenectomized for various pathological conditions. In all of them the LGL count was higher than 3.5 x 10(9)/l. No patient showed neutropenia nor suffered from rheumatoid arthritis. A surface markers heterogeneity was observed by immunophenotypic studies. A reversal of the CD4/CD8 ratio was observed in all patients, indicating that LGL are in the majority CD8+. Three patients showed the phenotype CD2+ CD3+ CD4- CD8+ indicating the T-lineage derivation of LGL; patient 6 showed a non-T non-B phenotype (CD2- CD3- CD4- CD8+/-). The percentage of lymphocytes presenting LGL-related markers (HNK-1, CD16, CD11b) was higher than that observed in normal subjects in 4 out of 5 examined patients. However, the percentage of cells bearing these markers was inferior to the LGL counts indicating that not all LGL express them. NK cytotoxic activity was similar to that of normal subjects in the three examined patients. Our data suggest that lymphocytosis of LGL in splenectomized subjects is a reactive process favoured by the asplenic state.
在6例因各种病理状况而接受脾切除术的患者中观察到了大颗粒淋巴细胞(LGL)淋巴细胞增多。所有患者的LGL计数均高于3.5×10⁹/L。没有患者出现中性粒细胞减少,也没有患者患有类风湿性关节炎。通过免疫表型研究观察到表面标志物的异质性。在所有患者中均观察到CD4/CD8比值的逆转,表明LGL大多数为CD8⁺。3例患者表现出CD2⁺ CD3⁺ CD4⁻ CD8⁺表型,表明LGL来源于T细胞系;患者6表现出非T非B表型(CD2⁻ CD3⁻ CD4⁻ CD8⁺/⁻)。在5例接受检查的患者中,有4例呈现LGL相关标志物(HNK-1、CD16、CD11b)的淋巴细胞百分比高于正常受试者。然而,携带这些标志物的细胞百分比低于LGL计数,这表明并非所有LGL都表达它们。在3例接受检查的患者中,NK细胞毒性活性与正常受试者相似。我们的数据表明,脾切除术后患者的LGL淋巴细胞增多是一种由无脾状态促进的反应性过程。