Ghaderkhani Sara, SeyedAlinaghi SeyedAhmad, Farhadi Kousha, Abbasian Ladan, Abdollahi Alireza, Hasannezhad Malihe, Dehghan Manshadi Seyed Ali, Rajabi Erta
Department of Infectious Disease and Tropical Medicine, School of Medicine, Iranian Research Center for HIV/AIDS, Iranian Institute for Reduction of High-Risk Behaviors, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran.
Iranian Research Center for HIV/AIDS, Iranian Institute for Reduction of High-Risk Behaviors, Tehran University of Medical Sciences, Tehran, Iran.
AIDS Res Ther. 2025 Apr 3;22(1):42. doi: 10.1186/s12981-025-00735-7.
The human immunodeficiency virus (HIV) increases susceptibility to measles, mumps, and rubella (MMR) infections due to decreased cluster of differentiation 4 + T-cell levels and rapid waning of protective antibodies following vaccination, which imposes a significant impact on HIV-positive women of reproductive age, for whom MMR vaccination is a crucial preventive measure. This study aimed to shed light on the immunity status of women of childbearing age with HIV infection post-MMR-vaccination during their childhood and the necessity of further vaccination in these individuals.
To evaluate seroconversion rates following vaccination through Iran's NIP or previous infection by assessing MMR IgG levels, all Iranian women aged 18-45 years referred to our voluntary counseling center, with or without HIV infection and CD4 levels 200 cells/mm or higher at the time of enrollment, were invited to participate. Data were collected through the Hospital Information System and questionnaires, and blood samples were taken to evaluate the seroconversion following MMR vaccination via NIP or previous MMR infection.
In this study, 150 women participated, with a mean age (± SD) of 36.49 (± 6.80). Mean rubella and measles IgG levels of HIV-positive participants (95.08 ± 79.42 IU/Ml) were higher than HIV-negative peers (8.98 ± 3.83 mg/dL) with no significant associations (p-value > 0.05). However, mumps IgG levels were significantly lower compared to HIV-negative participants (9.87 ± 28.70 mg/dL, p-value < 0.001). Additionally, HIV-positive participants significantly exhibited lower total immunity (n = 73, 97.3) compared to HIV-negative participants (n = 64, 85.3) (p-value = 0.07). HIV-positive individuals who did not have seroimmunity against mumps infection had significantly lower CD4 NADIR counts (cells/mm3) (mean ± SD = 259.00 ± 203.31, p-value: 0.025). Moreover, regression analyses demonstrated significant associations between decreased mumps IgG levels and lower CD4 NADIR counts (AOR = 1.004, 95% CI = 1-1.008, p value = 0.03).
Our research found that HIV-positive women may need MMR revaccination due to increased susceptibility to at least one of these viruses. We also highlighted the significance of considering lower CD4 NADIR as a risk factor for mumps development in women living with HIV infection.
由于分化簇4 + T细胞水平降低以及接种疫苗后保护性抗体迅速减弱,人类免疫缺陷病毒(HIV)会增加对麻疹、腮腺炎和风疹(MMR)感染的易感性,这对处于生育年龄的HIV阳性女性产生了重大影响,而MMR疫苗接种对她们来说是一项至关重要的预防措施。本研究旨在阐明曾在儿童期接种MMR疫苗的育龄HIV感染女性的免疫状况,以及这些个体进一步接种疫苗的必要性。
为了通过评估MMR IgG水平来评估通过伊朗国家免疫规划(NIP)接种疫苗后的血清转化率或既往感染情况,邀请了所有年龄在18 - 45岁、前往我们自愿咨询中心的伊朗女性参与,无论其是否感染HIV,且入组时CD4水平为200个细胞/mm³或更高。通过医院信息系统和问卷收集数据,并采集血样以评估通过NIP接种MMR疫苗后的血清转化率或既往MMR感染情况。
在本研究中,150名女性参与,平均年龄(±标准差)为36.49(±6.80)。HIV阳性参与者的风疹和麻疹IgG平均水平(95.08±79.42 IU/Ml)高于HIV阴性同龄人(8.98±3.83 mg/dL),但无显著相关性(p值>0.05)。然而,与HIV阴性参与者相比,腮腺炎IgG水平显著较低(9.87±28.70 mg/dL,p值<0.001)。此外,与HIV阴性参与者(n = 64,85.3)相比,HIV阳性参与者的总体免疫力显著较低(n = 73,97.3)(p值 = 0.07)。对腮腺炎感染无血清免疫的HIV阳性个体的CD4最低点计数(细胞/mm³)显著较低(平均值±标准差 = 259.00±203.31,p值:0.025)。此外,回归分析表明腮腺炎IgG水平降低与较低的CD4最低点计数之间存在显著关联(调整优势比 = 1.004,95%置信区间 = 1 - 1.008,p值 = 0.03)。
我们的研究发现,HIV阳性女性可能因对这些病毒中至少一种的易感性增加而需要再次接种MMR疫苗。我们还强调了将较低的CD4最低点视为HIV感染女性患腮腺炎风险因素的重要性。