Ahlstedt S
Scand J Infect Dis Suppl. 1980;Suppl 24:216-9.
The increase of the resistance against intraperitoneal (i.p.) Escherichia coli to infection was studied in immunized mice with or without immunosuppression with cyclophosphamide (Cy), or/and niridazole (Nir). These agents suppress antibody formation and T-cell mediated immunity respectively. An infection system was utilized permitting exclusive study of immunity against the 06 antigen. The antibody titers in serum were recorded with an enzyme-linked immunosorbent assay, ELISA. The following findings were made: (1) One immunization resulted in protection against i.p. E. coli 06 infection as well as in antibody titers measured with the ELISA. Two immunizations given with a 30-day interval increased the noted levels even more. (2) The resistance to infection after one immunization was fully transferable with immune serum; the resistance after two immunizations was not fully transferable with immune serum. (3) Treatment with cyclophosphamide diminished the antibody formation after immunization but not the resistance to infection. The resistance raised by one immunization was transferable by immune serum from immunosuppressed animals; the resistance raised by two immunizations was partly transferable bny such immune. (4) Treatment with niridazole, which inhibits T-cell mediated immunity, did not alone or in combination with cyclophosphamide affect the resistance pattern after immunization.
研究了在免疫小鼠中,无论有无用环磷酰胺(Cy)或/和硝唑咪(Nir)进行免疫抑制,腹腔内(i.p.)大肠杆菌感染抗性的增加情况。这些药物分别抑制抗体形成和T细胞介导的免疫。采用了一种感染系统,以便专门研究针对06抗原的免疫。用酶联免疫吸附测定法(ELISA)记录血清中的抗体滴度。得出以下结果:(1)一次免疫可提供针对腹腔内大肠杆菌06感染的保护,同时ELISA测得的抗体滴度也会升高。间隔30天进行两次免疫可使上述水平进一步提高。(2)一次免疫后的感染抗性可通过免疫血清完全转移;两次免疫后的抗性不能通过免疫血清完全转移。(3)环磷酰胺处理会减少免疫后的抗体形成,但不会降低感染抗性。一次免疫产生的抗性可由免疫抑制动物的免疫血清转移;两次免疫产生的抗性可部分由这种免疫血清转移。(4)抑制T细胞介导免疫的硝唑咪单独使用或与环磷酰胺联合使用,均不影响免疫后的抗性模式。