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猫房水中弓形虫特异性IgA的检测。

Detection of Toxoplasma gondii-specific IgA in the aqueous humor of cats.

作者信息

Lappin M R, Burney D P, Hill S A, Chavkin M J

机构信息

Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins 80523, USA.

出版信息

Am J Vet Res. 1995 Jun;56(6):774-8.

PMID:7653887
Abstract

Toxoplasma gondii-specific IgA, IgM, and IgG were measured by ELISA in the serum and aqueous humor of 29 client-owned cats with endogenous uveitis and 7 specific-pathogen-free cats tested sequentially for 20 weeks after inoculation with T gondii. Local antibody production in aqueous humor was estimated by multiplying the aqueous humor-to-serum T gondii-specific antibody ratio by the serum-to-aqueous humor total IgG (C value) or calicivirus-specific IgG (CTC value) ratio. Evidence for local production of antibody in aqueous humor was defined as C value greater than 8 or CTC value greater than 1. Toxoplasma gondii-specific IgM CTC values, IgG CTC values, or IgA CTC values greater than 1 were detected in the aqueous humor of 18 of 29 (62.1%) client-owned cats with endogenous uveitis; 2 cats had IgA CTC values greater than 1 without detectable IgM or IgG in aqueous humor. Toxoplasma gondii-specific IgM was not detected in the aqueous humor of experimentally inoculated cats before or after inoculation. Immunoglobulin G C values greater than 8 were detected in all 7 experimentally inoculated cats and ranged from 10.4 to 145.5. Immunoglobulin G C values greater than 8 were first detected 4 to 8 weeks after T gondii inoculation and were undetectable by week 16 after inoculation. Immunoglobulin A C values greater than 8 were detected in 4 of 7 cats and ranged from 12.7 to 264.3. Immunoglobulin A C values greater than 8 were first detected 4 to 8 weeks after inoculation, and were detected in 2 cats during week 20 after inoculation. It was concluded that some cats infected with T gondii develop detectable concentrations of T gondii-specific IgA in aqueous humor.

摘要

通过酶联免疫吸附测定法(ELISA)检测了29只患有内源性葡萄膜炎的客户拥有的猫以及7只无特定病原体猫的血清和房水中的弓形虫特异性IgA、IgM和IgG,这些无特定病原体猫在接种弓形虫后连续检测20周。通过将房水与血清弓形虫特异性抗体比值乘以血清与房水总IgG(C值)或杯状病毒特异性IgG(CTC值)比值来估计房水中局部抗体的产生。房水中抗体局部产生的证据定义为C值大于8或CTC值大于1。在29只患有内源性葡萄膜炎的客户拥有的猫中,有18只(62.1%)的房水中检测到弓形虫特异性IgM CTC值、IgG CTC值或IgA CTC值大于1;2只猫的IgA CTC值大于1,但房水中未检测到IgM或IgG。在实验接种的猫接种前或接种后的房水中均未检测到弓形虫特异性IgM。在所有7只实验接种的猫中均检测到IgG C值大于8,范围为10.4至145.5。IgG C值大于8在弓形虫接种后4至8周首次检测到,接种后第16周无法检测到。7只猫中有4只检测到IgA C值大于8,范围为12.7至264.3。IgA C值大于8在接种后4至8周首次检测到,接种后第20周在2只猫中检测到。得出的结论是,一些感染弓形虫的猫在房水中会产生可检测浓度的弓形虫特异性IgA。

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