Bhaumik Siddhartha Kumar, Singh Manoj Kumar, Karmakar Subir, De Tripti
Division of Infectious Disease and Immunology, Indian Institute of Chemical Biology, 4 Raja S.C. Mullick Road, Jadavpur, Kolkata, 700032, India.
Glycoconj J. 2009 Aug;26(6):663-73. doi: 10.1007/s10719-008-9212-y. Epub 2008 Nov 13.
As compared to cutaneous leishmaniasis, vaccination against visceral leishmaniasis (VL) has received limited attention. In this study, we demonstrate for the first time that an UDP-Galactose: N-acetylglucosamine beta 1-4 galactosyltransferase (GenBank Accession No. EF159943) expressing attenuated LD clonal population (A-LD) is able to confer protection against the experimental challenge with the virulent LD AG83 parasite. A-LD was also effective in established leishmania infection. The vaccinated animals showed both cell mediated (in vitro T-cell proliferation, and DTH response) and humoral responses (Th1 type). These results demonstrate the potential of the attenuated clones as an immunotherapeutic and immunoprophylactic agent against visceral leishmaniasis.
与皮肤利什曼病相比,针对内脏利什曼病(VL)的疫苗接种受到的关注有限。在本研究中,我们首次证明,表达UDP-半乳糖:N-乙酰葡糖胺β1-4半乳糖基转移酶(GenBank登录号EF159943)的减毒LD克隆群体(A-LD)能够抵御强毒LD AG83寄生虫的实验性攻击。A-LD在已建立的利什曼原虫感染中也有效。接种疫苗的动物表现出细胞介导的(体外T细胞增殖和迟发型超敏反应)和体液反应(Th1型)。这些结果证明了减毒克隆作为针对内脏利什曼病的免疫治疗和免疫预防剂的潜力。