Rogers Jeffrey M, Chentsova Victoria O, Wang Crystal X, Marcondes Maria Cecilia Garibaldi, Cherner Mariana, Ellis Ronald J, Letendre Scott L, Heaton Robert K, Grant Igor, Iudicello Jennifer E
San Diego State University/University of California San Diego Joint Doctoral Program in Clinical Psychology, San Diego, CA 92120, USA.
Department of Psychiatry, University of California San Diego, San Diego, CA 92093, USA.
Viruses. 2025 Aug 20;17(8):1143. doi: 10.3390/v17081143.
Methamphetamine use, which is disproportionately prevalent among people with HIV, increases risk for cardio- and neurovascular pathology through persistent immune activation and inflammation. Preclinical studies indicate that cannabinoids may reduce markers of pro-inflammatory processes, but data from people with chronic inflammatory conditions are limited. We examined potentially interacting associations of lifetime methamphetamine use disorder (MUD), recent cannabis use, and HIV with four plasma markers of immune and inflammatory functions.
Participants with HIV (PWH, = 86) and without HIV (PWoH, = 148) provided urine and blood samples and completed neuromedical, psychiatric, and substance use assessments. Generalized linear models examined main and conditional associations of lifetime MUD, past-month cannabis use, and HIV with plasma concentrations of CXCL10/IP-10, CCL2/MCP-1, ICAM-1, and VCAM-1.
PWH displayed higher CXCL10/IP-10 than PWoH. Past-month cannabis use was independently associated with lower CXCL10/IP-10 levels and conditionally lower CCL2/MCP-1, ICAM-1, and VCAM-1 levels among people with lifetime MUD, but only PWoH displayed cannabis-associated lower VCAM-1 levels.
Human plasma sample evidence suggests that cannabis use is associated with lower levels of immune and inflammatory molecules in the context of MUD or HIV. Cannabinoid pathways may be worthwhile clinical targets for treating sequelae of chronic inflammatory conditions.
甲基苯丙胺的使用在艾滋病毒感染者中极为普遍,通过持续的免疫激活和炎症增加了心血管和神经血管病变的风险。临床前研究表明,大麻素可能会降低促炎过程的标志物,但来自慢性炎症患者的数据有限。我们研究了终生甲基苯丙胺使用障碍(MUD)、近期大麻使用和艾滋病毒与四种免疫和炎症功能血浆标志物之间潜在的相互作用关联。
有艾滋病毒的参与者(PWH,n = 86)和无艾滋病毒的参与者(PWoH,n = 148)提供尿液和血液样本,并完成神经医学、精神病学和物质使用评估。广义线性模型研究了终生MUD、过去一个月大麻使用和艾滋病毒与CXCL10/IP - 10、CCL2/MCP - 1、ICAM - 1和VCAM - 1血浆浓度之间的主要和条件关联。
PWH的CXCL10/IP - 10水平高于PWoH。过去一个月使用大麻与终生患有MUD的人群中较低的CXCL10/IP - 10水平以及条件性较低的CCL2/MCP - 1、ICAM - 1和VCAM - 1水平独立相关,但只有PWoH显示出与大麻相关的较低VCAM - 1水平。
人体血浆样本证据表明,在MUD或艾滋病毒背景下,使用大麻与较低水平的免疫和炎症分子相关。大麻素途径可能是治疗慢性炎症后遗症的有价值的临床靶点。