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C型应对方式、述情障碍和心率反应性与与HIV进展相关的特定免疫机制独立且不同地相关联。

Type C coping, alexithymia, and heart rate reactivity are associated independently and differentially with specific immune mechanisms linked to HIV progression.

作者信息

Temoshok Lydia R, Waldstein Shari R, Wald Rebecca L, Garzino-Demo Alfredo, Synowski Stephen J, Sun Lingling, Wiley James A

机构信息

Institute of Human Virology, Department of Medicine, University of Maryland School of Medicine, 725 West Lombard Street, N 146, Baltimore, MD 21201, USA.

出版信息

Brain Behav Immun. 2008 Jul;22(5):781-92. doi: 10.1016/j.bbi.2008.02.003. Epub 2008 Mar 17.

Abstract

The maladaptive Type C coping style has been linked to disease progression in HIV and other immunologically mediated disorders. We hypothesized that strong Type C coping, higher levels of alexithymia, and greater cardiovascular (particularly heart rate) responses to, and prolonged recovery from stress would be associated with poorer functioning of immune parameters previously linked to HIV pathogenesis and progression: (1) antigen-stimulated production of the beta (beta)-chemokines MIP-1 alpha and MIP-1 beta, which bind to the HIV co-receptor CCR5 and block HIV entry into CD4(+) lymphocytes; and (2) antigen-stimulated production of the proinflammatory cytokine interleukin-6 (IL-6), which synergizes immune activation associated with HIV replication. We examined relations among psychological, cardiovascular, and immune variables in a baseline sample of 200 HIV-infected, predominantly African American outpatients attending an HIV primary care clinic in inner-city Baltimore. In regression analyses adjusted for CD4(+) count and age, strong Type C coping was associated with significantly higher IL-6 production, as predicted. The theoretically related construct of alexithymia was correlated with significantly lower stimulated production of HIV-inhibiting MIP-1 alpha. Independent of alexithymia, greater heart rate reactivity, and poorer heart rate recovery in response to experimental stressors were also significantly associated with lower production of MIP-1 alpha, adjusted for cardiovascular medications, methadone use, CD4(+) count, and age. These findings support our primary set of hypotheses that maladaptive Type C coping, alexithymia, and heart rate reactivity/recovery are associated with disturbances in two key immune parameters implicated in HIV pathogenesis. Our secondary hypothesis, that dysregulated heart rate reactivity may mediate the connections between Type C coping and/or alexithymia and IL-6/ MIP-1 alpha was not confirmed. The finding that Type C coping, alexithymia, and heart rate reactivity/recovery are associated independently and differentially with specific aspects of relevant immune functioning may reflect distinct biobehavioral pathways that contribute to HIV progression.

摘要

适应不良的C型应对方式已被证明与HIV及其他免疫介导疾病的病情进展有关。我们推测,强烈的C型应对方式、较高的述情障碍水平、对压力的更大心血管反应(尤其是心率)以及压力后的长时间恢复,将与先前与HIV发病机制和病情进展相关的免疫参数功能较差有关:(1)抗原刺激产生的β趋化因子MIP-1α和MIP-1β,它们与HIV共受体CCR5结合并阻止HIV进入CD4(+)淋巴细胞;(2)抗原刺激产生的促炎细胞因子白细胞介素-6(IL-6),它协同与HIV复制相关的免疫激活。我们在一个由200名主要为非裔美国人的HIV感染者组成的基线样本中,研究了心理、心血管和免疫变量之间的关系,这些患者在巴尔的摩市中心的一家HIV初级保健诊所就诊。在针对CD4(+)细胞计数和年龄进行调整的回归分析中,如预期的那样,强烈的C型应对方式与IL-6的产生显著增加有关。理论上与之相关的述情障碍结构与HIV抑制性MIP-1α的刺激产生显著降低相关。独立于述情障碍,在针对心血管药物使用、美沙酮使用、CD4(+)细胞计数和年龄进行调整后,对实验应激源的更大心率反应性和较差的心率恢复也与MIP-1α的产生显著降低相关。这些发现支持了我们的主要假设,即适应不良的C型应对方式、述情障碍和心率反应性/恢复与HIV发病机制中涉及的两个关键免疫参数的紊乱有关。我们的次要假设,即心率反应性失调可能介导C型应对方式和/或述情障碍与IL-6/MIP-1α之间的联系,未得到证实。C型应对方式、述情障碍和心率反应性/恢复与相关免疫功能的特定方面独立且不同地相关,这一发现可能反映了导致HIV病情进展的不同生物行为途径。

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