Castes M, Cabrera M, Trujillo D, Convit J
Instituto of Biomedicina, Escuela de Medicina J. M. Vargas, Universidad Central de Venezuela, Caracas.
J Clin Microbiol. 1988 Jun;26(6):1207-13. doi: 10.1128/jcm.26.6.1207-1213.1988.
Leukocyte subpopulations, the expression of the interleukin-2 (IL-2) receptor, and the production of IL-2 and gamma interferon (IFN-gamma) were studied in the peripheral blood mononuclear cells of American cutaneous leishmaniasis patients that had been stimulated in vitro with either leishmanial antigen or mitogen (phytohemagglutinin M). The 75 patients examined were classified as having either the localized (LCL; 66 patients), mucocutaneous (MCL; 5 patients), or the rare diffuse (DCL; 4 patients) form of the disease. Patients with DCL, who are characterized by their defective cell-mediated immune response to leishmanial antigen, failed to express the IL-2 receptor and did not produce IFN-gamma when exposed to the antigen but did so when stimulated by phytohemagglutinin M. Both LCL and MCL patients showed strong proliferative responses to leishmanial antigen; these were by far the greatest in MCL patients. Both groups had significantly increased IL-2 receptor expression and IFN-gamma production after exposure to either antigen or mitogen, and these were highest in the MCL patients. Concerning the leukocyte subpopulations evaluated (CD2, CD4, CD8, CD20, MO2), the most significant findings were a decrease of both CD4+ cells and the CD4/CD8 ratio in MCL patients compared with the other groups. Considering IL-2 production, in response to phytohemagglutinin M both MCL and LCL patients showed amounts of IL-2 comparable to those of the controls. Our results help explain the anergy of T cells from DCL patients to leishmanial antigen, which could lead to a defective production of IFN-gamma and possibly contribute to their incapacity to kill the Leishmania parasite. Concerning MCL patients, the significantly increased expression of IL-2 receptor, decreased expression of the CD4 (helper-inducer of suppression) phenotype, and elevated IFV-gamma production might partially explains the state of hypersensitivity and mucosal damage exhibited by these patients.
对美国皮肤利什曼病患者的外周血单个核细胞进行研究,观察其白细胞亚群、白细胞介素-2(IL-2)受体的表达以及IL-2和γ干扰素(IFN-γ)的产生情况。这些细胞在体外分别用利什曼原虫抗原或丝裂原(植物血凝素M)刺激。所检查的75例患者被分类为患有局部型(LCL;66例患者)、黏膜皮肤型(MCL;5例患者)或罕见的弥漫型(DCL;4例患者)疾病。DCL患者的特征是对利什曼原虫抗原的细胞介导免疫反应存在缺陷,在接触抗原时未能表达IL-2受体且不产生IFN-γ,但在植物血凝素M刺激下则会表达和产生。LCL和MCL患者对利什曼原虫抗原均表现出强烈的增殖反应;其中MCL患者的反应最为强烈。两组患者在接触抗原或丝裂原后,IL-2受体表达和IFN-γ产生均显著增加;MCL患者的增加幅度最大。关于所评估的白细胞亚群(CD2、CD4、CD8、CD20、MO2),最显著的发现是与其他组相比,MCL患者的CD4 +细胞和CD4/CD8比值均降低。考虑到IL-2的产生,MCL和LCL患者在对植物血凝素M的反应中所产生的IL-2量与对照组相当。我们的结果有助于解释DCL患者的T细胞对利什曼原虫抗原的无反应性,这可能导致IFN-γ产生缺陷,并可能导致其无法杀死利什曼原虫。关于MCL患者,IL-2受体表达显著增加、CD4(辅助诱导抑制)表型表达降低以及IFV-γ产生升高,可能部分解释了这些患者所表现出的超敏反应和黏膜损伤状态。