Chiplunkar S V, Deshmukh M A, Kode J A, Gangal S G, Deo M G
Cellular Immunology Division, Cancer Research Institute, Tata Memorial Centre, Bombay, India.
Acta Leprol. 1997;10(4):203-8.
Lymphokine-activated killer (LAK) cells were generated by interleukin-2 activation of peripheral blood lymphocytes obtained from lepromatous leprosy (LL) patients and healthy individuals. The ability of LAK cells to lyse targets (macrophages and T-24, a bladder carcinoma cell line) infected with mycobacteria (Mycobacterium leprae and mycobacterial strain ICRC) was assessed in a 51 chromium-release assay. It was observed that LAK cells generated from LL patients and healthy individuals could preferentially lyse M. leprae or ICRC-pulsed macrophages and T-24 cells, compared to non-pulsed targets. The ability of LAK cells to kill intracellular mycobacteria was demonstrated in colony forming assays. These results indicate a promising role for LAK cells in immunotherapy of leprosy.
通过白细胞介素-2激活从瘤型麻风(LL)患者和健康个体获取的外周血淋巴细胞来产生淋巴因子激活的杀伤(LAK)细胞。在51铬释放试验中评估LAK细胞裂解感染分枝杆菌(麻风分枝杆菌和分枝杆菌菌株ICRC)的靶细胞(巨噬细胞和膀胱癌细胞系T-24)的能力。观察到,与未脉冲处理的靶细胞相比,从LL患者和健康个体产生的LAK细胞可优先裂解经麻风分枝杆菌或ICRC脉冲处理的巨噬细胞和T-24细胞。在集落形成试验中证明了LAK细胞杀灭细胞内分枝杆菌的能力。这些结果表明LAK细胞在麻风病免疫治疗中具有广阔前景。