Santos Patrícia d'Emery Alves, Lorena Virgínia Maria Barros, Fernandes Érica, Sales Iana Rafaela Fernandes, Albuquerque Mônica Camelo Pessoa, Gomes Yara, Costa Vlaudia Maria Assis, Souza Valdênia Maria Oliveira
Laboratory of Immunology, Laboratory of Immunopathology Keizo Asami (LIKA), Federal University of Pernambuco, Recife, PE, Brazil.
Aggeu Magalhães Research Center (CPqAM), Oswaldo Cruz Foundation (FIOCRUZ), Recife, PE, Brazil.
Exp Parasitol. 2014 Jun;141:62-7. doi: 10.1016/j.exppara.2014.03.017. Epub 2014 Mar 21.
Adult offspring of Schistosoma mansoni-infected mice showed alterations in immunity to a heterologous antigen, ovalbumin (OA). Prior breastfeeding induced increased production of anti-OA antibodies, while pregnancy impaired it. Here, we investigated the expression of costimulatory molecules on antigen-presenting cells (APCs) of the adult offspring of S. mansoni-infected mothers in response to OA. Newborn mice were divided into three groups: animals Born Infected Mothers (BIM) suckled by non-infected mothers; animals from non-infected mothers Suckled Infected Mothers (SIM); and another group of mice born from and suckled by non-infected mothers (CONTROL). The adult offspring were immunized with subcutaneous OA+adjuvant, and 3-8days following immunization, double labeling was performed (CD45R/B220 or CD11c and CD80, CD86, CD40 or HLA-DR) on spleen cells. In comparison to the CONTROL group, an early increased frequency of CD40+/CD80+ B cells was observed in SIM mice (p<0.001/p<0.05), but no alteration of CD11c+ cells was observed. In contrast, in BIM mice, the frequency of CD86+/CD11c+ cells (p<0.05) and CD40+/CD80+/CD86+ B cells (p<0.01/p<0.01/p<0.05) was drastically reduced. In conclusion, previous suckling by S. mansoni-infected mothers enabled improved antigen presentation by B cells in adult offspring, whereas gestation in these mothers imprinted offspring with weak antigen presentation by APCs during the immune response to a non-related antigen.
曼氏血吸虫感染小鼠的成年子代对异源抗原卵清蛋白(OA)的免疫反应出现了改变。早期母乳喂养可诱导抗OA抗体产生增加,而怀孕则会损害这种反应。在此,我们研究了曼氏血吸虫感染母亲的成年子代抗原呈递细胞(APC)上共刺激分子对OA的反应性表达。新生小鼠分为三组:由未感染母亲哺乳的感染母亲所生动物(BIM);由感染母亲哺乳的未感染母亲所生动物(SIM);以及另一组由未感染母亲所生并由其哺乳的小鼠(对照组)。成年子代皮下注射OA+佐剂进行免疫,免疫后3 - 8天,对脾细胞进行双重标记(CD45R/B220或CD11c以及CD80、CD86、CD40或HLA - DR)。与对照组相比,SIM小鼠中CD40+/CD80+ B细胞频率早期增加(p<0.001/p<0.05),但未观察到CD11c+细胞有改变。相反,在BIM小鼠中,CD86+/CD11c+细胞频率(p<0.05)以及CD40+/CD80+/CD86+ B细胞频率(p<0.01/p<0.01/p<0.05)大幅降低。总之,先前由曼氏血吸虫感染的母亲哺乳可使成年子代中的B细胞更好地呈递抗原,而这些母亲的妊娠使子代在对非相关抗原的免疫反应中APC呈递抗原的能力较弱。