PMID- 24328935 OWN - NLM STAT- MEDLINE DCOM- 20140728 LR - 20131216 IS - 1557-8976 (Electronic) IS - 0882-8245 (Linking) VI - 26 IP - 6 DP - 2013 Dec TI - Positive inductive effect of swine interleukin-4 on immune responses elicited by modified live porcine reproductive and respiratory syndrome virus (PRRSV) vaccine. PG - 404-14 LID - 10.1089/vim.2013.0040 [doi] AB - Porcine reproductive and respiratory syndrome (PRRS) has become one of the most economically important diseases to the global pork industry. Currently, the efficacies of available commercial vaccines remain questionable: the modified live-PRRSV vaccines (MLVs) were generally effective but variable in sufficient protection, and the outcomes of inactivated-PRRSV vaccines (IVs) in the field were not very promising. In the present study, we investigated the effect of swine interleukin 4 (IL-4) on the development of virus-specific immune responses elicited by an MLV. The antibody titer against PRRSV membrane proteins in pigs elicited by MLV plus recombinant plasmid encoding IL-4 (group 3) was significantly higher than those elicited by MLV alone (group 1) and MLV plus empty plasmid (group 2) from 35 days post-inoculation (dpi). Similarly, the neutralizing efficacy of sera from group 3 was markedly enhanced compared with group 1 and group 2. In cellular immunity, the ratio of CD3(+)CD4(+)/CD3(+)CD8(+) T lymphocyte subpopulations from group 3 monitored by flow cytometry (FCM) was significantly higher than those from group 1 and group 2 from 42 dpi to 21 days post-challenge (dpc). After viral challenge, pigs in group 3 showed significantly lower virus loads in peripheral blood measured by a real-time quantitative PCR (RT-qPCR), as compared with those in group 1 and group 2. Pigs in group 1 and group 2 had a low fever and displayed mild inappetence, lethargy, rough hair coats, and no lung lesions, while those in group 3 showed almost no clinical signs, no lung lesions. The scores of clinical signs of pigs in group 3 were significantly lower than those in both group 1 and group 2. Interestingly, the scores of lung lesions showed no significant differences among the three groups. Our results indicate that swine IL-4 markedly enhanced the protective immune response of pigs and improved the efficacy of the MLV in preventing PRRS disease. FAU - Peng, Jun AU - Peng J AD - 1 College of Veterinary Medicine, Shandong Agricultural University , Taian, China . FAU - Wang, Jinbao AU - Wang J FAU - Wu, Jiaqiang AU - Wu J FAU - Du, Yijun AU - Du Y FAU - Li, Jun AU - Li J FAU - Guo, Zhongkun AU - Guo Z FAU - Yu, Jiang AU - Yu J FAU - Xu, Shaojian AU - Xu S FAU - Zhang, Yuyu AU - Zhang Y FAU - Sun, Wenbo AU - Sun W FAU - Cong, Xiaoyan AU - Cong X FAU - Shi, Jianli AU - Shi J LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Viral Immunol JT - Viral immunology JID - 8801552 RN - 0 (Adjuvants, Immunologic) RN - 0 (Antibodies, Neutralizing) RN - 0 (Antibodies, Viral) RN - 0 (Vaccines, Attenuated) RN - 0 (Viral Vaccines) RN - 207137-56-2 (Interleukin-4) SB - IM MH - Adjuvants, Immunologic/*administration & dosage/genetics/*pharmacology MH - Animals MH - Antibodies, Neutralizing/blood MH - Antibodies, Viral/blood MH - CD4-Positive T-Lymphocytes/immunology MH - CD8-Positive T-Lymphocytes/immunology MH - Flow Cytometry MH - Interleukin-4/*administration & dosage/genetics/*pharmacology MH - Plasmids/administration & dosage MH - Porcine Reproductive and Respiratory Syndrome/pathology/prevention & control/virology MH - Porcine respiratory and reproductive syndrome virus/*immunology MH - Severity of Illness Index MH - Swine MH - T-Lymphocyte Subsets/immunology MH - Vaccines, Attenuated/administration & dosage/immunology MH - Viral Load MH - Viral Vaccines/*administration & dosage/*immunology MH - Viremia/prevention & control EDAT- 2013/12/18 06:00 MHDA- 2014/07/30 06:00 CRDT- 2013/12/17 06:00 PHST- 2013/12/17 06:00 [entrez] PHST- 2013/12/18 06:00 [pubmed] PHST- 2014/07/30 06:00 [medline] AID - 10.1089/vim.2013.0040 [doi] PST - ppublish SO - Viral Immunol. 2013 Dec;26(6):404-14. doi: 10.1089/vim.2013.0040.