ZERO WORLD RESEARCHアミノ酸・有機酸の学術文献データベース

L-arginine deprivation impairs Leishmania major-specific T-cell responses.

European journal of immunology2009Munder M, Choi BS, Rogers M, et al.
研究デザインその他の原著論文
対象動物

記録の確認項目

研究デザイン
その他の原著論文
対象
動物
出版年
2009
出典
doi.org
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表示あり
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有効な記録
状態確認日
2026/08/17
収集日
2026/08/13
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確認段階
自動処理
記録状態
公開

抄録

The amino acid L-arginine plays a crucial role in the regulation of immune responses. We have recently shown that uncontrolled replication of Leishmania parasites at the site of pathology correlates with high levels of arginase activity in nonhealing leishmaniasis and that this elevated arginase activity causes local depletion of L-arginine. To further our understanding of the impact of L-arginine deprivation in experimental leishmaniasis, here we characterize in detail the effects of L-arginine deprivation on antigen-specific T cells and MPhi. The results of our study show that decrease of L-arginine levels in the extracellular milieu affects the biological activities of Leishmania major-specific T cells, both at the level of the magnitude and the quality of their responses. L. major-specific CD4(+) T cells rendered hyporesponsive by L-arginine deprivation can be partially rescued by addition of exogenous L-arginine to produce IL-4 and IL-10, but not to produce IFN-gamma. Furthermore, our results show that L-arginine deprivation also greatly impacts parasite growth in activated macrophages. In summary, our results suggest that L-arginine levels affect both Th cell responses and parasite replication.

MeSH

AnimalsArginaseArginineCD4-Positive T-LymphocytesCell ProliferationFemaleFlow CytometryHost-Parasite InteractionsInterferon-gammaInterleukin-10Interleukin-4Leishmania majorLeishmaniasis, CutaneousMacrophagesMiceMice, Inbred BALB CMice, Inbred CBAT-Lymphocytes

DOI 10.1002/eji.200839041

PMID 19637195

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