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Effects of Short-Term Probiotic Ingestion on Immune Profiles and Microbial Translocation among HIV-1-Infected Vietnamese Children
Here, we investigated the effects of the probiotic strain Lactobacillus casei Shirota (LcS) on immune profiles and intestinal microbial translocation among children infected with human immunodeficiency virus (HIV). This prospective study included 60 HIV-infected children—including 31 without antiret...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666866/ https://www.ncbi.nlm.nih.gov/pubmed/29048352 http://dx.doi.org/10.3390/ijms18102185 |
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author | Ishizaki, Azumi Bi, Xiuqiong Nguyen, Lam Van Matsuda, Kazunori Pham, Hung Viet Phan, Chung Thi Thu Khu, Dung Thi Khanh Ichimura, Hiroshi |
author_facet | Ishizaki, Azumi Bi, Xiuqiong Nguyen, Lam Van Matsuda, Kazunori Pham, Hung Viet Phan, Chung Thi Thu Khu, Dung Thi Khanh Ichimura, Hiroshi |
author_sort | Ishizaki, Azumi |
collection | PubMed |
description | Here, we investigated the effects of the probiotic strain Lactobacillus casei Shirota (LcS) on immune profiles and intestinal microbial translocation among children infected with human immunodeficiency virus (HIV). This prospective study included 60 HIV-infected children—including 31 without antiretroviral therapy (ART) (HIV(+)) and 29 who received ART for a median of 3.5 years (ART(+)) and 20 children without HIV infection (HIV(−)). Participants were recruited in Vietnam. All children were given fermented milk containing LcS (6.5 × 10(9) cfu) daily for 8 weeks. Before and after LcS ingestion, blood samples were collected for virological, immunological, and bacteriological analyses. After LcS ingestion, peripheral CD4(+) T-cell and Th2 (CXCR3(−)CCR6(−)CD4(+)) counts significantly increased in both HIV-infected groups; Th17 (CXCR3(−)CCR6(+)CD4(+)) counts increased in all three groups; regulatory T-cell (CD25(high)CD4(+)) counts decreased in the ART(+) and HIV(−) groups; activated CD8(+) cells (CD38(+)HLA-DR(+)CD8(+)) decreased from 27.5% to 13.2% (p < 0.001) in HIV(+) children; and plasma HIV load decreased slightly but significantly among HIV(+) children. No group showed a significantly altered frequency of bacterial 16S/23S rRNA gene detection in the plasma. No serious adverse events occurred. These findings suggest that short-term LcS ingestion is a safe supportive approach with immunological and virological benefits in HIV-infected children. |
format | Online Article Text |
id | pubmed-5666866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56668662017-11-09 Effects of Short-Term Probiotic Ingestion on Immune Profiles and Microbial Translocation among HIV-1-Infected Vietnamese Children Ishizaki, Azumi Bi, Xiuqiong Nguyen, Lam Van Matsuda, Kazunori Pham, Hung Viet Phan, Chung Thi Thu Khu, Dung Thi Khanh Ichimura, Hiroshi Int J Mol Sci Article Here, we investigated the effects of the probiotic strain Lactobacillus casei Shirota (LcS) on immune profiles and intestinal microbial translocation among children infected with human immunodeficiency virus (HIV). This prospective study included 60 HIV-infected children—including 31 without antiretroviral therapy (ART) (HIV(+)) and 29 who received ART for a median of 3.5 years (ART(+)) and 20 children without HIV infection (HIV(−)). Participants were recruited in Vietnam. All children were given fermented milk containing LcS (6.5 × 10(9) cfu) daily for 8 weeks. Before and after LcS ingestion, blood samples were collected for virological, immunological, and bacteriological analyses. After LcS ingestion, peripheral CD4(+) T-cell and Th2 (CXCR3(−)CCR6(−)CD4(+)) counts significantly increased in both HIV-infected groups; Th17 (CXCR3(−)CCR6(+)CD4(+)) counts increased in all three groups; regulatory T-cell (CD25(high)CD4(+)) counts decreased in the ART(+) and HIV(−) groups; activated CD8(+) cells (CD38(+)HLA-DR(+)CD8(+)) decreased from 27.5% to 13.2% (p < 0.001) in HIV(+) children; and plasma HIV load decreased slightly but significantly among HIV(+) children. No group showed a significantly altered frequency of bacterial 16S/23S rRNA gene detection in the plasma. No serious adverse events occurred. These findings suggest that short-term LcS ingestion is a safe supportive approach with immunological and virological benefits in HIV-infected children. MDPI 2017-10-19 /pmc/articles/PMC5666866/ /pubmed/29048352 http://dx.doi.org/10.3390/ijms18102185 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ishizaki, Azumi Bi, Xiuqiong Nguyen, Lam Van Matsuda, Kazunori Pham, Hung Viet Phan, Chung Thi Thu Khu, Dung Thi Khanh Ichimura, Hiroshi Effects of Short-Term Probiotic Ingestion on Immune Profiles and Microbial Translocation among HIV-1-Infected Vietnamese Children |
title | Effects of Short-Term Probiotic Ingestion on Immune Profiles and Microbial Translocation among HIV-1-Infected Vietnamese Children |
title_full | Effects of Short-Term Probiotic Ingestion on Immune Profiles and Microbial Translocation among HIV-1-Infected Vietnamese Children |
title_fullStr | Effects of Short-Term Probiotic Ingestion on Immune Profiles and Microbial Translocation among HIV-1-Infected Vietnamese Children |
title_full_unstemmed | Effects of Short-Term Probiotic Ingestion on Immune Profiles and Microbial Translocation among HIV-1-Infected Vietnamese Children |
title_short | Effects of Short-Term Probiotic Ingestion on Immune Profiles and Microbial Translocation among HIV-1-Infected Vietnamese Children |
title_sort | effects of short-term probiotic ingestion on immune profiles and microbial translocation among hiv-1-infected vietnamese children |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5666866/ https://www.ncbi.nlm.nih.gov/pubmed/29048352 http://dx.doi.org/10.3390/ijms18102185 |
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