Gaspari A A, Lotze M T, Rosenberg S A, Stern J B, Katz S I
JAMA. 1987 Sep 25;258(12):1624-9.
We have prospectively evaluated the skin changes that occurred in ten patients who were undergoing immunotherapy with interleukin 2 (IL-2) and autologous lymphokine-activated killer cells to treat cancer. Serial skin biopsy specimens were obtained before therapy (baseline), during IL-2 administration, and during IL-2/lymphokine-activated killer cell infusion. All patients developed an eruption that was characterized by macular erythema, with burning and pruritus of the skin. It began after two or three days of IL-2 infusion and was usually localized to the head and neck; it occasionally became generalized (ie, erythroderma). The eruption resolved with desquamation within 48 to 72 hours after cessation of infusion of IL-2. Histologically, the changes were not specific. The only consistent immunohistological finding noted was the presence of DR+/Leu-4+ lymphoid cells surrounding blood vessels in the papillary dermis, with fewer of these cells in the epidermis. There was no difference between the clinical or histological features of the eruption that occurred with IL-2 alone and that which occurred with IL-2 and lymphokine-activated killer cell infusion, suggesting that the cutaneous effects were mediated by IL-2 alone.
我们前瞻性地评估了10名接受白细胞介素2(IL-2)和自体淋巴因子激活的杀伤细胞免疫治疗癌症的患者所出现的皮肤变化。在治疗前(基线)、IL-2给药期间以及IL-2/淋巴因子激活的杀伤细胞输注期间获取系列皮肤活检标本。所有患者均出现了以斑疹性红斑为特征的皮疹,伴有皮肤烧灼感和瘙痒。皮疹在IL-2输注两到三天后开始,通常局限于头颈部;偶尔会泛发(即红皮病)。在停止输注IL-2后48至72小时内,皮疹随脱屑而消退。组织学上,这些变化并不具有特异性。唯一一致的免疫组织学发现是在乳头真皮层血管周围存在DR+/Leu-4+淋巴细胞,而表皮中这些细胞较少。单独使用IL-2时出现的皮疹与使用IL-2和淋巴因子激活的杀伤细胞输注时出现的皮疹在临床或组织学特征上没有差异,这表明皮肤效应仅由IL-2介导。