Abelman Rebecca A, Fitzpatrick Jessica, Zawedde Josephine, Beck-Engeser Gabriele, Rn Ingvar Sanyu, Marzan Florence, Byanyima Patrick, Ambayec Gabrielle C, Kaswabuli Sylvia, Musisi Emmanuel, Sessolo Abdulwahab, Velasquez Elinor, Lalitha Rejani, Byanova Katerina L, Aweeka Francesca T, Deitchman Amelia N, Lin Jue, Davis J Lucian, Crothers Kristina, Worodria William, Hunt Peter W, Huang Laurence
Division of HIV, Infectious Diseases, and Global Medicine, Department of Medicine, University of California San Francisco, San Francisco, California, USA.
Infectious Diseases Research Collaboration, Kampala, Uganda.
J Acquir Immune Defic Syndr. 2025 Jun 18. doi: 10.1097/QAI.0000000000003713.
While there are sex and HIV differences in tuberculosis (TB) prevalence, the underlying mechanisms are incompletely understood. Few studies have evaluated whether sex and HIV modify the inflammatory response to TB.
Adults with pulmonary TB with and without HIV in Kampala, Uganda had 12 immune activation biomarkers measured at TB diagnosis and at completion of therapy. Associations between biomarkers and sex were assessed using multivariable regression models at baseline and follow-up after adjusting for age, HIV status, and AFB smear grade. Given evidence of sex-HIV interaction in several biomarkers, models were stratified by HIV status.
Overall, 151 participants were included and 74 (49%) were female. Forty-nine (32%) participants had HIV; 21 (43%) of those with HIV were female. At baseline, biomarkers were overall higher in men whereas at follow-up, suPAR (p<0.001) and sCD163 were higher in women (p=0.02) and IL-6 (p=0.01) and IFABP (p=0.02) were higher in men. After stratifying by HIV status, at baseline, the majority of the biomarkers were higher in men without HIV and there were no sex differences in those with HIV. At follow-up, women without HIV had higher levels of suPAR (p=0.01) and sCD163 (p=0.051). Women with HIV had higher levels of suPAR, CRP, and IP-10 (p<0.05 for all); no other sex differences were observed.
Among adults with pulmonary TB in Uganda, men had greater immune activation than women only in the absence of HIV. Following treatment, women tended to have more immune activation than men in the setting of HIV.
虽然结核病(TB)患病率存在性别和HIV差异,但其潜在机制尚未完全明确。很少有研究评估性别和HIV是否会改变对结核病的炎症反应。
在乌干达坎帕拉,对患有和未患有HIV的成年肺结核患者在结核病诊断时和治疗结束时测量了12种免疫激活生物标志物。在调整年龄、HIV状态和抗酸杆菌涂片等级后,使用多变量回归模型在基线和随访时评估生物标志物与性别的关联。鉴于几种生物标志物存在性别-HIV相互作用的证据,模型按HIV状态分层。
总共纳入了151名参与者,其中74名(49%)为女性。49名(32%)参与者感染了HIV;其中21名(43%)感染HIV的参与者为女性。在基线时,男性的生物标志物总体上更高,而在随访时,女性的可溶性尿激酶型纤溶酶原激活物受体(suPAR,p<0.001)和可溶性CD163更高(p=0.02),男性的白细胞介素-6(IL-6,p=0.01)和肠脂肪酸结合蛋白(IFABP,p=0.02)更高。按HIV状态分层后,在基线时,大多数生物标志物在未感染HIV的男性中更高,而感染HIV的男性和女性之间没有性别差异。在随访时,未感染HIV的女性suPAR(p=0.01)和可溶性CD163水平更高(p=0.051)。感染HIV的女性suPAR、C反应蛋白(CRP)和干扰素γ诱导蛋白10(IP-10)水平更高(均p<0.05);未观察到其他性别差异。
在乌干达成年肺结核患者中,仅在未感染HIV的情况下男性的免疫激活程度高于女性。治疗后,在感染HIV的情况下女性的免疫激活程度往往高于男性。