Tiwary B K, Goel M C
Vet Immunol Immunopathol. 1984 Oct;7(3-4):305-13. doi: 10.1016/0165-2427(84)90088-6.
Four different protocols were tested for the induction of IgA deficiency in chickens: (I) inoculation of anti-alpha intra-peritoneally (i.p.) on alternate days after hatching up to a period of three weeks; (II) bursectomy within 6 h and at 24 h after hatching; (III) in-ovo injection of anti-alpha on the 17th day of embryonation followed by bursectomy at 24 h of hatch and a single injection of anti-alpha i.p. on the day of hatching; (IV) as in III above but bursectomy within 6 h of hatch, followed by three further injections of anti-alpha on days 3, 10 and 34 after hatching. Treatment (I) produced temporary dysgammaglobulinemia during the period of treatment. Bursectomy at 24 h of hatch rendered 75% of the chicks IgA deficient up to four weeks of age. Early bursectomy within 6 h of hatch resulted in substantial improvement of IgA suppression. Such chicks, when tested at 4, 6 and 10 weeks of age, were found to be 81, 72 and 58.3% IgA deficient, respectively. With treatment (III) all the treated birds were IgA deficient at four weeks of age. However, as the birds grew older, IgA appeared in the serum so that at the age of 12 weeks only 27.3% were deficient. Treatment (IV) completely suppressed the IgA system of 13 out of 14 chickens. These chickens lacked both serum and secretory IgA as well as IgA-containing cells in their intestinal mucosa. Both IgG and IgM continued to be produced.
对四种不同的方案进行了测试,以诱导鸡的IgA缺乏症:(I)在孵化后每隔一天腹腔内(i.p.)接种抗α,持续三周;(II)在孵化后6小时和24小时进行法氏囊切除术;(III)在胚胎发育的第17天进行卵内注射抗α,然后在孵化后24小时进行法氏囊切除术,并在孵化当天腹腔内单次注射抗α;(IV)与上述(III)相同,但在孵化后6小时内进行法氏囊切除术,随后在孵化后第3、10和34天再进行三次抗α注射。处理(I)在处理期间产生了暂时性的γ球蛋白异常血症。在孵化后24小时进行法氏囊切除术,使75%的雏鸡在四周龄前IgA缺乏。在孵化后6小时内进行早期法氏囊切除术导致IgA抑制有显著改善。这些雏鸡在4、6和10周龄时进行测试,分别发现81%、72%和58.3%的雏鸡IgA缺乏。采用处理(III),所有处理过的鸡在四周龄时均IgA缺乏。然而,随着鸡龄的增长,血清中出现了IgA,因此在12周龄时只有27.3%的鸡缺乏IgA。处理(IV)完全抑制了14只鸡中13只鸡的IgA系统。这些鸡既缺乏血清IgA和分泌型IgA,也缺乏肠道黏膜中含IgA的细胞。IgG和IgM仍继续产生。