Beaulieu L, Beaudoin J, Jobin M, Hébert J
Int Arch Allergy Appl Immunol. 1986;79(3):249-52. doi: 10.1159/000233981.
Histamine is known to modulate immune responses through the induction of suppressor cell subsets. The inhibition studies with antagonists suggest that the H2 agonist accounts for most of the suppression. This work studies the effects of various concentrations of 3-methyl histamine (as negative control), histamine, and pure H1 (2-methyl histamine, 2-pyridyl ethylamine) and H2 (4-methyl histamine, dimaprit) receptor agonists on the mitogenic (phytohemagglutinin A) proliferative response of normal human lymphocytes. At high concentrations of agonists (10(-3), 10(-4) M) the suppression induced by the two types of agonists is comparable to that of histamine. At lower concentrations (10(-6) M) the suppression is seen only in the presence of the H2 agonist. The suppression induced by the two agonists is generally reversed in the presence of an H2 receptor antagonist. The H1 receptor antagonist did not abolish and even increased the suppression induced by histamine and the two agonists.
已知组胺可通过诱导抑制性细胞亚群来调节免疫反应。使用拮抗剂的抑制研究表明,H2激动剂是大部分抑制作用的原因。这项工作研究了不同浓度的3-甲基组胺(作为阴性对照)、组胺以及纯H1(2-甲基组胺、2-吡啶乙胺)和H2(4-甲基组胺、二甲双胍)受体激动剂对正常人淋巴细胞有丝分裂(植物血凝素A)增殖反应的影响。在高浓度激动剂(10⁻³、10⁻⁴ M)时,两种类型激动剂诱导的抑制作用与组胺相当。在较低浓度(10⁻⁶ M)时,仅在存在H2激动剂的情况下才出现抑制作用。两种激动剂诱导的抑制作用在H2受体拮抗剂存在时通常会逆转。H1受体拮抗剂并未消除甚至增强了组胺和两种激动剂诱导的抑制作用。