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印度城市地区重症恶性疟患者的1型人类免疫缺陷病毒感染

Human immunodeficiency virus type 1 infection in patients with severe falciparum malaria in urban India.

作者信息

Khasnis A A, Karnad D R

机构信息

Department of Medicine, K. E. M. Hospital, Parel, Mumbai - 400012, India.

出版信息

J Postgrad Med. 2003 Apr-Jun;49(2):114-7.

Abstract

BACKGROUND

CD4+ T cells restrict parasitaemia during the first attack of falciparum malaria; humoral immunity, develops weeks later and protects against reinfection. HIV infection may affect severity of falciparum malaria and development of protective immunity.

AIMS

To study the prevalence of HIV infection in Indian patients with severe falciparum malaria and its effect on severity of illness and recurrences of and mortality related to malarial infection.

PATIENTS

Consecutive patients with severe falciparum malaria and voluntary blood donors.

SETTING AND DESIGN

Prospective cohort study in a university hospital in Mumbai.

RESULTS

Five (11.6%) of 43 patients and 521 (1.8%) of 28749 blood donors had HIV infection (OR 7.1, 95% CI = 2.8 to 18.2, p=0.001). Clinical features, APACHE II score, number of organs affected, parasite index and mortality in patients with and without HIV infection were comparable. CD4+ counts were < 500 cells/ microl in 2 patients and normal in 3. Opportunistic infections including pulmonary tuberculosis in one patient (CD4+ counts > 500 cells/ microl), and oral candidiasis in two (CD4+ counts 275 and 250 cells/ microl) were noted. One patient developed fatal Pneumocystis carinii pneumonia two weeks after recovering from malaria. P. falciparum infection recurred in 2 of the 4 HIV infected survivors and in none of 31 survivors without HIV infection (RR 38.8, 95% CI 2.2 to 671, p=0.01).

CONCLUSIONS

HIV infection is associated with increased risk of severe malaria even with normal CD4+ counts; severity of disease and mortality are not increased. However, prior HIV infection impairs protective immune response to Plasmodium falciparum in residents of hypoendemic areas.

摘要

背景

在恶性疟原虫首次发作期间,CD4 + T细胞限制寄生虫血症;体液免疫在数周后发展并预防再次感染。HIV感染可能影响恶性疟原虫疟疾的严重程度和保护性免疫的发展。

目的

研究印度重症恶性疟原虫疟疾患者中HIV感染的患病率及其对疾病严重程度、疟疾感染复发率和死亡率的影响。

患者

连续的重症恶性疟原虫疟疾患者和自愿献血者。

地点和设计

在孟买一家大学医院进行的前瞻性队列研究。

结果

43例患者中有5例(11.6%)和28749名献血者中有521例(1.8%)感染了HIV(比值比7.1,95%可信区间=2.8至18.2,p = 0.001)。有HIV感染和无HIV感染患者的临床特征、急性生理与慢性健康状况评分系统II评分、受影响器官数量、寄生虫指数和死亡率相当。2例患者的CD4 + 细胞计数<500个/微升,3例正常。观察到1例机会性感染(CD4 + 细胞计数>500个/微升)为肺结核,2例(CD4 + 细胞计数分别为275和250个/微升)为口腔念珠菌病。1例患者在疟疾康复两周后发生致命的卡氏肺孢子虫肺炎。4例HIV感染幸存者中有2例恶性疟原虫感染复发,31例无HIV感染的幸存者中无一例复发(相对危险度38.8,95%可信区间2.2至671,p = 0.01)。

结论

即使CD4 + 细胞计数正常,HIV感染也与重症疟疾风险增加相关;疾病严重程度和死亡率并未增加。然而,既往HIV感染会损害低流行地区居民对恶性疟原虫的保护性免疫反应。

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