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Chemiluminescent responses of alveolar macrophages from normal and Mycobacterium bovis BCG-vaccinated rabbits as a function of age.

作者信息

Chida K, Myrvik Q N, Leake E S, Gordon M R, Wood P H, Ricardo M J

出版信息

Infect Immun. 1987 Jun;55(6):1476-83. doi: 10.1128/iai.55.6.1476-1483.1987.

DOI:10.1128/iai.55.6.1476-1483.1987
PMID:3553004
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC260539/
Abstract

Luminol-dependent chemiluminescence (CL) responses of alveolar macrophages (AM) from normal and Mycobacterium bovis BCG-vaccinated infant and adult rabbits were compared. AM from 1-, 7-, and 14-day-old normal rabbits exhibited much lower peak CL responses than did AM from 28- and 42-day-old normal animals as well as rabbits 2 to 3 or 5 to 6 months and 1 to 2 years of age. The most striking differences among AM from infant and adult rabbits were noted when AM were obtained from 28-day-old and 5- to 6-month old rabbits 21 days after the rabbits were immunized with 200 micrograms of BCG intravenously. In this case, AM from 5- to 6-month-old animals gave peak counts per minute of 400,000 to 500,000 whereas AM from 28-day-old rabbits vaccinated with BCG (harvested at 49 days of age) gave peak counts per minute of only 40,715 +/- 2,688. These data reveal that AM from neonatal animals are grossly deficient as responders to phorbol myristate acetate-induced CL. This deficiency, which improved with age, is still apparent in AM from 28-day-old animals. The data also reveal that BCG vaccination of 28-day-old animals yields AM that are poor responders to phorbol myristate acetate compared with AM from BCG-vaccinated animals 2 to 3 and 5 to 6 months of age. AM from animals vaccinated with BCG at 28 days of age contained fewer and smaller electron-dense lysosomelike structures than did AM from adult rabbits similarly vaccinated. These findings provide an explanation for the difficulties infants have in developing effective cell-mediated immune responses against intracellular parasites.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbe/260539/164c1c1f8545/iai00090-0151-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbe/260539/37d4617d99d2/iai00090-0150-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbe/260539/866943357d90/iai00090-0151-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbe/260539/164c1c1f8545/iai00090-0151-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbe/260539/37d4617d99d2/iai00090-0150-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbe/260539/866943357d90/iai00090-0151-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3dbe/260539/164c1c1f8545/iai00090-0151-b.jpg

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本文引用的文献

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The measurement of opsonic and phagocytic function by Luminol-dependent chemiluminescence.通过鲁米诺依赖的化学发光法测定调理吞噬功能。
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Primary structures of MCP-1 and MCP-2, natural peptide antibiotics of rabbit lung macrophages.兔肺巨噬细胞天然肽抗生素MCP - 1和MCP - 2的一级结构
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Antibacterial activity of microbicidal cationic proteins 1 and 2, natural peptide antibiotics of rabbit lung macrophages.杀菌阳离子蛋白1和2的抗菌活性,兔肺巨噬细胞的天然肽抗生素。
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Infect Immun. 1984 Jul;45(1):1-5. doi: 10.1128/iai.45.1.1-5.1984.
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Pseudomonas aeruginosa exoproteases inhibit human neutrophil chemiluminescence.铜绿假单胞菌外蛋白酶抑制人类中性粒细胞化学发光。
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J Immunol. 1983 Nov;131(5):2104-6.
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Unsaturated fatty acids as second messengers of superoxide generation by macrophages.不饱和脂肪酸作为巨噬细胞产生超氧化物的第二信使。
Cell Immunol. 1983 Jul 15;79(2):240-52. doi: 10.1016/0008-8749(83)90067-9.
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Effect of in vitro preincubation of polymorphonuclear leukocytes on formylmethionyl-leucyl-phenylalanine-induced chemiluminescence.多形核白细胞体外预孵育对甲酰甲硫氨酰-亮氨酰-苯丙氨酸诱导的化学发光的影响。
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