Thompson G, Naqi S
Department of Avian and Aquatic Animal Medicine, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.
Avian Dis. 1997 Jul-Sep;41(3):690-4.
Previously uninoculated control chickens and chickens exposed to infectious bursal disease virus (IBDV) at 1 day of age were intranasally exposed to the M41 strain of infectious bronchitis virus (IBV) at 5 wk of age. Between 7 and 13 days after inoculation with IBV, cells were collected from the respiratory tracts of both groups of chickens and assayed for in vitro cytotoxic activity against a lymphoblastoid LSCC-RP9 target cell line using a 4-hr 51chromium-release assay (CRA). Compared to thymocytes from uninfected chickens, which were used as negative controls in the CRA, respiratory tract cells from both groups consistently displayed significant cytotoxic activity against LSCC-RP9 target cells. This cytotoxic activity, attributed to natural killer cells, was statistically more pronounced (P < 0.05) in IBDV plus IBV-infected chickens than in chickens inoculated with IBV alone.
先前未接种的对照鸡和1日龄时接触传染性法氏囊病病毒(IBDV)的鸡,在5周龄时经鼻接触传染性支气管炎病毒(IBV)的M41株。在接种IBV后7至13天之间,从两组鸡的呼吸道收集细胞,并使用4小时51铬释放试验(CRA)测定其对淋巴母细胞样LSCC-RP9靶细胞系的体外细胞毒性活性。与在CRA中用作阴性对照的未感染鸡的胸腺细胞相比,两组的呼吸道细胞对LSCC-RP9靶细胞始终表现出显著的细胞毒性活性。这种归因于自然杀伤细胞的细胞毒性活性,在感染IBDV加IBV的鸡中比仅接种IBV的鸡在统计学上更明显(P<0.05)。