{"title":"冷藏、室温和处理时间对神经元性肌囊炎血清免疫荧光抗体效价的影响。","authors":"Claudia Valderrama-Martinez, Andrea Packham, Shichen Zheng, Woutrina Smith, Magdalena Plancarte, Monica Aleman","doi":"10.1111/jvim.17282","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Evaluating antibody titers for <i>Sarcocystis neurona</i> for the diagnosis of equine protozoal myeloencephalitis from serum samples is a common practice. However, ensuring timely and proper refrigeration is not always possible.</p>\n </section>\n \n <section>\n \n <h3> Objectives</h3>\n \n <p>To evaluate immunofluorescent antibody (IFA) titers for <i>S. neurona</i> from serum samples stored at room temperature and 4°C.</p>\n </section>\n \n <section>\n \n <h3> Samples</h3>\n \n <p>Twenty-two serum samples.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Prospective longitudinal study. Two serum aliquots of 1 mL each were stored at room temperature (20-23.3°C) and 4°C. The unrefrigerated aliquot was immediately tested for IFA titers. Both aliquots were retested on Days 5 and 10 after collection. A paired <i>t</i> test was used to compare IFA titers at different time points.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>There was no significant difference between IFA titers from baseline with those stored at room temperature at Days 5 (<i>P</i> = .741, 95% CI [−56.83, 78.65]), 10 (<i>P</i> = .677, 95% CI [−50.01, 75.46]), and between 5 and 10 days (<i>P</i> = 0.949, 95% CI [−57.50, 61.14]). There was no significant difference from baseline with those stored at 4°C for Days 5 (<i>P</i> = .964, 95% CI [−81.81, 85.45]), 10 (<i>P</i> = 0.573, 95% CI [−109.4, 62.15]), and between 5 and 10 days (<i>P</i> = .5, 95% CI [−102.6, 51.67]). There was no statistical difference between samples stored at room temperature and 4°C (<i>P</i> = .688, CI [−55.51, 37.33]) on Days 5 and 10 (<i>P</i> = .104, CI [−80.8, 8.07]).</p>\n </section>\n \n <section>\n \n <h3> Conclusions and Clinical Importance</h3>\n \n <p>Immunofluorescent antibody test titers for <i>S. neurona</i> are stable for up to 10 days at room temperature and 4°C.</p>\n </section>\n </div>","PeriodicalId":49958,"journal":{"name":"Journal of Veterinary Internal Medicine","volume":"39 1","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11665959/pdf/","citationCount":"0","resultStr":"{\"title\":\"Effect of refrigeration, room temperature, and processing time on serum immunofluorescent antibody titers for Sarcocystis neurona\",\"authors\":\"Claudia Valderrama-Martinez, Andrea Packham, Shichen Zheng, Woutrina Smith, Magdalena Plancarte, Monica Aleman\",\"doi\":\"10.1111/jvim.17282\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Evaluating antibody titers for <i>Sarcocystis neurona</i> for the diagnosis of equine protozoal myeloencephalitis from serum samples is a common practice. However, ensuring timely and proper refrigeration is not always possible.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Objectives</h3>\\n \\n <p>To evaluate immunofluorescent antibody (IFA) titers for <i>S. neurona</i> from serum samples stored at room temperature and 4°C.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Samples</h3>\\n \\n <p>Twenty-two serum samples.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>Prospective longitudinal study. Two serum aliquots of 1 mL each were stored at room temperature (20-23.3°C) and 4°C. The unrefrigerated aliquot was immediately tested for IFA titers. Both aliquots were retested on Days 5 and 10 after collection. A paired <i>t</i> test was used to compare IFA titers at different time points.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>There was no significant difference between IFA titers from baseline with those stored at room temperature at Days 5 (<i>P</i> = .741, 95% CI [−56.83, 78.65]), 10 (<i>P</i> = .677, 95% CI [−50.01, 75.46]), and between 5 and 10 days (<i>P</i> = 0.949, 95% CI [−57.50, 61.14]). There was no significant difference from baseline with those stored at 4°C for Days 5 (<i>P</i> = .964, 95% CI [−81.81, 85.45]), 10 (<i>P</i> = 0.573, 95% CI [−109.4, 62.15]), and between 5 and 10 days (<i>P</i> = .5, 95% CI [−102.6, 51.67]). There was no statistical difference between samples stored at room temperature and 4°C (<i>P</i> = .688, CI [−55.51, 37.33]) on Days 5 and 10 (<i>P</i> = .104, CI [−80.8, 8.07]).</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions and Clinical Importance</h3>\\n \\n <p>Immunofluorescent antibody test titers for <i>S. neurona</i> are stable for up to 10 days at room temperature and 4°C.</p>\\n </section>\\n </div>\",\"PeriodicalId\":49958,\"journal\":{\"name\":\"Journal of Veterinary Internal Medicine\",\"volume\":\"39 1\",\"pages\":\"\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2024-12-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11665959/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Veterinary Internal Medicine\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/jvim.17282\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"VETERINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Veterinary Internal Medicine","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jvim.17282","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"VETERINARY SCIENCES","Score":null,"Total":0}
Effect of refrigeration, room temperature, and processing time on serum immunofluorescent antibody titers for Sarcocystis neurona
Background
Evaluating antibody titers for Sarcocystis neurona for the diagnosis of equine protozoal myeloencephalitis from serum samples is a common practice. However, ensuring timely and proper refrigeration is not always possible.
Objectives
To evaluate immunofluorescent antibody (IFA) titers for S. neurona from serum samples stored at room temperature and 4°C.
Samples
Twenty-two serum samples.
Methods
Prospective longitudinal study. Two serum aliquots of 1 mL each were stored at room temperature (20-23.3°C) and 4°C. The unrefrigerated aliquot was immediately tested for IFA titers. Both aliquots were retested on Days 5 and 10 after collection. A paired t test was used to compare IFA titers at different time points.
Results
There was no significant difference between IFA titers from baseline with those stored at room temperature at Days 5 (P = .741, 95% CI [−56.83, 78.65]), 10 (P = .677, 95% CI [−50.01, 75.46]), and between 5 and 10 days (P = 0.949, 95% CI [−57.50, 61.14]). There was no significant difference from baseline with those stored at 4°C for Days 5 (P = .964, 95% CI [−81.81, 85.45]), 10 (P = 0.573, 95% CI [−109.4, 62.15]), and between 5 and 10 days (P = .5, 95% CI [−102.6, 51.67]). There was no statistical difference between samples stored at room temperature and 4°C (P = .688, CI [−55.51, 37.33]) on Days 5 and 10 (P = .104, CI [−80.8, 8.07]).
Conclusions and Clinical Importance
Immunofluorescent antibody test titers for S. neurona are stable for up to 10 days at room temperature and 4°C.
期刊介绍:
The mission of the Journal of Veterinary Internal Medicine is to advance veterinary medical knowledge and improve the lives of animals by publication of authoritative scientific articles of animal diseases.