Gupta R K, Maheshwari S C, Singh H
J Biol Stand. 1985 Apr;13(2):151-7. doi: 10.1016/s0092-1157(85)80021-4.
Two methods of fixation of sheep erythrocytes with formaldehyde for the titration of tetanus antitoxin by the indirect haemagglutination (IHA) test have been compared. The cells fixed with 3% formaldehyde at 4-8 degrees C for 24 h (formaldehyde (I) fixed cells) were less sensitive than the cells fixed with 3% formaldehyde at 4-8 degrees C for 24 h and subsequently treated with 40% formaldehyde at 4-8 degrees C for a further 24 h (formaldehyde (II) fixed cells). The correlation between the toxin neutralization (TN) and IHA titres using formaldehyde (I) fixed cells was better than that obtained with formaldehyde (II) fixed cells. There was no statistically significant difference between TN and IHA titres after treatment of the sera with 2-Mercaptoethanol using formaldehyde (I) fixed cells. Formaldehyde (I) fixed cells can be used for two months with adequate sensitivity to detect the minimum protective level of tetanus antitoxin in the sera.
比较了两种用甲醛固定绵羊红细胞以通过间接血凝试验(IHA)滴定破伤风抗毒素的方法。在4 - 8℃用3%甲醛固定24小时的细胞(甲醛(I)固定细胞)比在4 - 8℃用3%甲醛固定24小时,随后在4 - 8℃再用40%甲醛处理24小时的细胞(甲醛(II)固定细胞)敏感性更低。使用甲醛(I)固定细胞时,毒素中和(TN)滴度与IHA滴度之间的相关性优于使用甲醛(II)固定细胞时。使用甲醛(I)固定细胞,用2 - 巯基乙醇处理血清后,TN和IHA滴度之间无统计学显著差异。甲醛(I)固定细胞可使用两个月,具有足够的敏感性以检测血清中破伤风抗毒素的最低保护水平。