Clements J D, Hartzog N M, Lyon F L
Department of Microbiology and Immunology, Tulane University Medical Center, New Orleans, Louisiana.
Vaccine. 1988 Jun;6(3):269-77. doi: 10.1016/0264-410x(88)90223-x.
The ability of Escherichia coli heat-labile enterotoxin (LT) to influence the induction and maintenance of tolerance was examined in animals primed orally with a soluble protein antigen, ovalbumin (OVA), or in animals primed orally with two unrelated protein antigens administered simultaneously, OVA and bovine serum albumin (BSA). LT is immunologically and structurally related to the cholera enterotoxin (CT), which has been shown to be capable of abrogating oral tolerance to protein antigens when delivered simultaneously with the antigens. In this study, simultaneous administration of LT with OVA was shown to prevent the induction of tolerance to OVA and to increase the serum anti-OVA IgG response 30- to 90-fold over OVA-primed and PBS-primed animals, respectively. This effect was determined to be a function of the enzymatically active A subunit of the toxin since the B (binding) subunit alone was unable to influence tolerance induction. Animals fed LT with OVA after the initial OVA prime developed a significantly lower serum IgG and mucosal IgA anti-OVA response than those fed LT with OVA in the initial immunization, indicating that prior exposure to the antigen reduces the effectiveness of LT to influence tolerance and its ability to act as an adjuvant. LT was not able to abrogate tolerance once it had been established. Serum IgG and mucosal IgA responses in animals receiving LT on only a single occasion, that being upon first exposure to antigen, were equivalent to responses after three OVA/LT primes, indicating that commitment to responsiveness occurs early and upon first exposure to antigen.(ABSTRACT TRUNCATED AT 250 WORDS)
在经口用可溶性蛋白抗原卵清蛋白(OVA)致敏的动物,或经口同时给予两种不相关蛋白抗原(OVA和牛血清白蛋白(BSA))致敏的动物中,检测了大肠杆菌不耐热肠毒素(LT)影响耐受性诱导和维持的能力。LT在免疫和结构上与霍乱肠毒素(CT)相关,已证明当与抗原同时递送时,CT能够消除对蛋白抗原的口服耐受性。在本研究中,OVA与LT同时给药可阻止对OVA耐受性的诱导,并使血清抗OVA IgG反应分别比OVA致敏和PBS致敏的动物增加30至90倍。该作用被确定为毒素酶活性A亚基的功能,因为单独的B(结合)亚基无法影响耐受性诱导。在初次用OVA致敏后给动物喂食OVA与LT,其血清IgG和粘膜IgA抗OVA反应明显低于初次免疫时喂食OVA与LT的动物,这表明预先接触抗原会降低LT影响耐受性的有效性及其作为佐剂的能力。一旦建立耐受性,LT就无法消除它。仅在首次接触抗原时单次接受LT的动物的血清IgG和粘膜IgA反应与三次OVA/LT致敏后的反应相当,这表明对反应性的承诺在首次接触抗原时就早早发生了。(摘要截短至250字)