Evans Dwight L, Ten Have Thomas R, Douglas Steven D, Gettes David R, Morrison Mary, Chiappini Margaret S, Brinker-Spence Priscilla, Job Carla, Mercer Delinda E, Wang Yan Lin, Cruess Dean, Dube Benoit, Dalen Erik A, Brown Tiffany, Bauer Russell, Petitto John M
Department of Psychiatry, University of Pennsylvania School of Medicine, 305 Blockley Hall, Philadelphia, PA 19104-6021, USA.
Am J Psychiatry. 2002 Oct;159(10):1752-9. doi: 10.1176/appi.ajp.159.10.1752.
Clinical and epidemiology studies have implicated depression as a risk factor in the morbidity and mortality of many human diseases. This study sought to determine if depression was associated with alterations in cellular immunity variables-specifically, natural killer (NK) cells and CD8 T lymphocytes-in women with HIV infection.
Ninety-three women (63 HIV-seropositive, 30 HIV-seronegative) were studied as part of an ongoing longitudinal study conducted at two sites. Subjects underwent extensive clinical, psychiatric, and immunological evaluations. CBC counts and flow cytometry panels were conducted and NK cell activity assayed for all subjects; viral load was determined for HIV-seropositive subjects.
The overall rate of major depression in the HIV-seropositive and HIV-seronegative women was 15.87% (N=10 of 63) and 10.00% (N=3 of 30), respectively. HIV-seropositive women had higher depressive symptom scores than did the comparison subjects (Hamilton depression scale: mean=8.62 [SD=7.26] versus mean=5.67 [SD=7.33], respectively). Both groups had similar anxiety scores. Depressive and anxiety symptoms were significantly associated with higher activated CD8 T lymphocyte counts and higher viral load levels. Major depression was associated with significantly lower natural killer cell activity, and depressive and anxiety symptom scores showed a similar correlation.
Our findings provide the first evidence that depression may alter the function of killer lymphocytes in HIV-infected women and suggest that depression may decrease natural killer cell activity and lead to an increase in activated CD8 T lymphocytes and viral load. The rate of current major depression in these HIV-seropositive women (none of whom had current substance abuse) is approximately twice that reported for HIV-seropositive men. The rate is also consistent with studies of women with other medical illnesses and with a recent epidemiology study that associated depression with mortality in HIV-infected women with chronic depressive symptoms. Depression may have a negative impact on innate immunity. Examination of killer lymphocytes may prove useful in assessing the potential relationship between depression, immunity, and HIV disease progression in women.
临床和流行病学研究表明,抑郁症是许多人类疾病发病和死亡的危险因素。本研究旨在确定抑郁症是否与HIV感染女性的细胞免疫变量改变有关,特别是自然杀伤(NK)细胞和CD8 T淋巴细胞。
作为在两个地点进行的一项正在进行的纵向研究的一部分,对93名女性(63名HIV血清阳性,30名HIV血清阴性)进行了研究。受试者接受了广泛的临床、精神和免疫学评估。对所有受试者进行全血细胞计数和流式细胞术检测,并测定NK细胞活性;对HIV血清阳性受试者测定病毒载量。
HIV血清阳性和HIV血清阴性女性的重度抑郁症总体发生率分别为15.87%(63人中10人)和10.00%(30人中3人)。HIV血清阳性女性的抑郁症状评分高于对照组(汉密尔顿抑郁量表:平均值分别为8.62[标准差=7.26]和5.67[标准差=7.33])。两组的焦虑评分相似。抑郁和焦虑症状与活化的CD8 T淋巴细胞计数升高和病毒载量水平升高显著相关。重度抑郁症与自然杀伤细胞活性显著降低相关,抑郁和焦虑症状评分也显示出类似的相关性。
我们的研究结果首次证明,抑郁症可能会改变HIV感染女性杀伤淋巴细胞的功能,并表明抑郁症可能会降低自然杀伤细胞活性,导致活化的CD8 T淋巴细胞和病毒载量增加。这些HIV血清阳性女性(均无当前药物滥用情况)目前的重度抑郁症发生率约为HIV血清阳性男性报告发生率的两倍。该发生率也与其他疾病女性的研究以及最近一项将抑郁症与有慢性抑郁症状的HIV感染女性死亡率相关联的流行病学研究一致。抑郁症可能对先天免疫有负面影响。检查杀伤淋巴细胞可能有助于评估抑郁症、免疫和HIV疾病在女性中进展之间的潜在关系。