Casal M L, Jezyk P F, Giger U
Department of Clinical Studies, School of Veterinary Medicine, University of Pennsylvania, Philadelphia 19104-6010, USA.
Am J Vet Res. 1996 Nov;57(11):1653-8.
To examine systemic immunity in kittens, including transfer of maternal immunoglobulins from the queen to kittens, and subsequent decay of passively obtained immunoglobulins.
6 healthy queens and their 46 kittens.
Immunoglobulin concentrations were measured in serum, colostrum, and milk of queens and in their kittens' sera. Decay rate constants and half-lives of maternally derived immunoglobulins were determined. To determine intestinal absorption, foreign IgG was given to kittens at 6- to 8-hour intervals after birth, and bovine IgM was given to kittens at birth.
Immunoglobulin concentrations of milk and colostrum did not differ significantly after removal of milk fat. Mean IgG concentration was higher in colostrum/ milk, whereas mean IgA and IgM concentrations were lower than those in the queens' serum. No IgG or IgA was detected in any of the precolostral serum samples obtained from kittens. Small amounts of IgM were present in the sera from 5 kittens at birth. Transferred IgG and IgA decreased rapidly with half-lives of 4.4 +/- 3.57 and 1.93 +/- 1.94 days, respectively. Serum IgM concentration increased irregularly during the first week of life, followed by a steady increase. Foreign IgG given up to 12 hours after birth was detected in kittens' serum, whereas IgG given at or after 16 hours was not found in any kitten's serum.
Milk and colostral immunoglobulin concentrations did not differ significantly. The half-lives of maternally derived IgG and IgA in kittens were shorter than those reported in dogs. IgG given at or after 16 hours of life was not absorbed by neonatal kittens.
Queen's milk obtained anytime during lactation may be used as a replacement for colostrum as a source of antibodies for neonatal kittens. Kittens at risk for neonatal isoerythrolysis must only be removed from the queens during the first day of life.
研究幼猫的全身免疫,包括母体免疫球蛋白从母猫向幼猫的转移,以及被动获得的免疫球蛋白随后的衰减情况。
6只健康母猫及其46只幼猫。
测定母猫血清、初乳和乳汁以及幼猫血清中的免疫球蛋白浓度。确定母体来源免疫球蛋白的衰减速率常数和半衰期。为了确定肠道吸收情况,在幼猫出生后6至8小时间隔给予外源IgG,并在出生时给予牛IgM。
去除乳脂后,乳汁和初乳中的免疫球蛋白浓度无显著差异。初乳/乳汁中的平均IgG浓度较高,而平均IgA和IgM浓度低于母猫血清中的浓度。从幼猫获得的任何初乳前血清样本中均未检测到IgG或IgA。出生时,5只幼猫的血清中存在少量IgM。转移的IgG和IgA迅速下降,半衰期分别为4.4±3.57天和1.93±1.94天。出生后第一周血清IgM浓度不规则增加,随后稳步上升。出生后12小时内给予的外源IgG在幼猫血清中被检测到,而在16小时或之后给予的IgG在任何幼猫血清中均未发现。
乳汁和初乳中的免疫球蛋白浓度无显著差异。幼猫体内母体来源的IgG和IgA半衰期比犬类报道的要短。出生后16小时或之后给予的IgG未被新生幼猫吸收。
哺乳期任何时候获得的母猫乳汁都可作为初乳的替代品,作为新生幼猫的抗体来源。有新生仔畜溶血病风险的幼猫必须仅在出生第一天与母猫分离。