Khaled Nagwa, Gaghan Carissa, Fares Abdelhamid M, Goodell Christa, Stanley William, Kulkarni Raveendra R, Gimeno Isabel M
College of Veterinary Medicine, North Carolina State University, Raleigh, NC 27607, USA.
Faculty of Veterinary Medicine, University of Sadat City, El Sadat City 6011007, Menofia Governorate, Egypt.
Pathogens. 2025 Jan 10;14(1):54. doi: 10.3390/pathogens14010054.
Very virulent plus Marek's disease virus (vv+MDV) induces severe immunosuppression in commercial chickens. In this study, we evaluated how three Gallid alphaherpesvirus 2 (GaHV-2) vaccines (CVI-988, rMd5-BAC∆Meq, and CVI-LTR) protected against two negative outcomes of vv+MDV infection: (1) reduced viability and frequency of immune cells in the spleen and (2) decreased efficacy of the CEO (chicken embryo origin) vaccine against infectious laryngotracheitis challenge. At 25 days post-infection with vv+MDV 686, all vaccines are protected against the reduced viability of splenocytes. However, there were differences in the frequency of splenic immunophenotypes among groups. Compared to the uninfected control, the frequency of B cells was reduced in the CVI-988/686 group but not in the rMd5-BAC∆Meq/686 and CVI-LTR/686 groups. T cell subset frequencies showed no difference between the negative controls and CVI-988/686; however, there was a reduction in activated CD4+ T cells in the rMd5-BAC∆Meq/686 group and in activated CD4+, activated CD8+, and γδ+ T cells in the CVI-LTR/686 group. We also demonstrated that the three vaccines protected against MDV-induced tumors, but only rMd5-BAC∆Meq and CVI-LTR protected against the negative impact of vv+MDV 648A strain on CEO vaccine efficacy. Our findings demonstrate important differences in the biology and/or mechanisms of protection of these vaccines.
超强毒力马立克氏病病毒(vv+MDV)可在商品鸡中诱导严重的免疫抑制。在本研究中,我们评估了三种鸡α疱疹病毒2型(GaHV-2)疫苗(CVI-988、rMd5-BAC∆Meq和CVI-LTR)如何预防vv+MDV感染的两个负面结果:(1)脾脏中免疫细胞活力和频率降低;(2)鸡胚源(CEO)疫苗针对传染性喉气管炎攻击的效力降低。在感染vv+MDV 686后25天,所有疫苗都能预防脾细胞活力降低。然而,各组间脾脏免疫表型频率存在差异。与未感染对照组相比,CVI-988/686组B细胞频率降低,但rMd5-BAC∆Meq/686组和CVI-LTR/686组未降低。阴性对照组与CVI-988/686组之间T细胞亚群频率无差异;然而,rMd5-BAC∆Meq/686组活化CD4+T细胞减少,CVI-LTR/686组活化CD4+、活化CD8+和γδ+T细胞减少。我们还证明,这三种疫苗可预防MDV诱导的肿瘤,但只有rMd5-BAC∆Meq和CVI-LTR可预防vv+MDV 648A毒株对CEO疫苗效力的负面影响。我们的研究结果表明这些疫苗在生物学和/或保护机制上存在重要差异。