Shum D T, Galsworthy S B
Immunology. 1982 Jun;46(2):343-51.
A monocytosis-producing activity (MPA) is present in a saline-extractable material (SE) from Listeria monocytogenes. The mechanism of stimulation of monocyte production by SE was studied. Serum obtained from mice at appropriate times after injection of SE induced monocytosis in normal recipients. The monocytosis-inducing activity present in serum differed from SE with respect to timing of the monocytosis, fractionation pattern on a Sephadex G-200 column, and thermolability. The minimum dose of SE capable of producing a monocytosis was 100 micrograms. Antibody to SE capable of detecting SE at a concentration of greater than 5 micrograms/ml failed to detect SE in samples of active serum. Therefore it seemed highly unlikely that activity in serum was due to the presence of trace amounts of SE. The activity present in serum was thermolabile and had a molecular weight of about 38,000. The data are consistent with the hypothesis that injection of SE caused the production or release of an endogenous mediator capable of stimulating monocytosis.
产单核细胞增多活性(MPA)存在于单核细胞增生李斯特菌的盐提取物(SE)中。对SE刺激单核细胞生成的机制进行了研究。在注射SE后适当时间从小鼠获得的血清可诱导正常受体产生单核细胞增多。血清中存在的单核细胞增多诱导活性在单核细胞增多的时间、在葡聚糖G - 200柱上的分级分离模式以及热稳定性方面与SE不同。能够产生单核细胞增多的SE的最小剂量为100微克。能够在浓度大于5微克/毫升时检测到SE的SE抗体未能在活性血清样本中检测到SE。因此,血清中的活性极不可能是由于痕量SE的存在。血清中存在的活性是热不稳定的,分子量约为38,000。这些数据与以下假设一致,即注射SE导致能够刺激单核细胞增多的内源性介质的产生或释放。