Soulez B, Palluault F, Dei-Cas E, Aliouat E M, Camus D
INSERM (U.42), Villeneuve d'Ascq, France.
J Protozool. 1991 Nov-Dec;38(6):189S-190S.
A colony of BALB/c mice maintained in a protected area of our laboratory was not infected with Pneumocystis carinii. During corticosteroid treatment, animals became infected by exposure to infected mice. After four months of corticosteroid treatment, BALB/c mice developed severe pneumocystosis. Stopping of treatment was associated with: (i) high mortality of mice, (ii) decreased lung parasite level and (iii) appearance of anti-P. carinii antibodies in survivors. A monoclonal antibody (MAb) 4F2 was obtained by immortalisation of spleen lymphocytes of a female BALB/c mouse 3 months after the cessation of corticosteroid treatment. The MAb 4F2 recognized a 210-220 kDa mouse P. carinii antigen, but did not react with rat-, rabbit- or human-derived P. carinii. This MAb reacted with all stages of mouse P. carinii.
我们实验室保护区内饲养的一群BALB/c小鼠未感染卡氏肺孢子虫。在皮质类固醇治疗期间,这些动物因接触感染小鼠而被感染。经过四个月的皮质类固醇治疗后,BALB/c小鼠出现了严重的肺孢子虫病。停止治疗后出现了以下情况:(i)小鼠死亡率高,(ii)肺部寄生虫水平降低,(iii)存活小鼠体内出现抗卡氏肺孢子虫抗体。在停止皮质类固醇治疗3个月后,通过使一只雌性BALB/c小鼠的脾淋巴细胞永生化获得了单克隆抗体(MAb)4F2。MAb 4F2识别一种210 - 220 kDa的小鼠卡氏肺孢子虫抗原,但不与大鼠、兔或人源的卡氏肺孢子虫发生反应。这种单克隆抗体与小鼠卡氏肺孢子虫的所有阶段均发生反应。