Gut microbiome variations during hematopoietic stem cell transplant in severe combined immunodeficiency.

Jonathan P. Lane; Christopher Stewart; Stephen Cummings; Andrew R. Gennery

doi:10.1016/j.jaci.2015.01.024

Gut microbiome variations during hematopoietic stem cell transplant in severe combined immunodeficiency.

Jonathan P. Lane, Christopher Stewart, Stephen Cummings, Andrew R. Gennery

Research output: Contribution to journal › Article › peer-review

Abstract

The composition of the gut microbiome is unstable in infancy,1
with many environmental factors determining its development including mode of delivery, method of feeding, antibiotic exposure, and neonatal hospitalisation.2
Severe combined immunodeficiency (SCID), a primary T-lymphocyte immunodeficiency causing severe viral infections, Pneumocystis jiroveci pneumonitis, chronic diarrhea, and failure to thrive, is fatal in infancy without hematopoietic stem cell transplantation (HSCT). Once diagnosed, children with SCID receive prolonged courses of antibiotics and breast-feeding frequently ceases during this critical time for gut microbiome development.3
Chemotherapeutic conditioning often precedes HSCT and can cause mucositis and severe immunosuppression, increasing the risk of bacteremia. HSCT can be complicated by graft-versus-host-disease (GvHD) causing severe gut inflammation. In HSCT in adults, overgrowth by a dominant gut microbiome species and the subsequent reduced diversity have been associated with gut GvHD4
, 5
and bacteremia.6
However, the gut microbiome in HSCT in infancy, specifically in SCID, has not been explored.

Original language	English
Pages (from-to)	1654-1656
Journal	The Journal of allergy and clinical immunology
Volume	135
Issue number	6
DOIs	https://doi.org/10.1016/j.jaci.2015.01.024
Publication status	Published - 12 Mar 2015

Access to Document

10.1016/j.jaci.2015.01.024Licence: Unspecified

Fingerprint Dive into the research topics of 'Gut microbiome variations during hematopoietic stem cell transplant in severe combined immunodeficiency.'. Together they form a unique fingerprint.

Stephen Cummings
- S.Cummings@tees.ac.uk
- National Horizons Centre
- SHLS Senior Executive Team - Dean
Person: Senior Management

Cite this

@article{2ef293b3a818448f954cbfc326936d6f,

title = "Gut microbiome variations during hematopoietic stem cell transplant in severe combined immunodeficiency.",

abstract = "The composition of the gut microbiome is unstable in infancy,1with many environmental factors determining its development including mode of delivery, method of feeding, antibiotic exposure, and neonatal hospitalisation.2Severe combined immunodeficiency (SCID), a primary T-lymphocyte immunodeficiency causing severe viral infections, Pneumocystis jiroveci pneumonitis, chronic diarrhea, and failure to thrive, is fatal in infancy without hematopoietic stem cell transplantation (HSCT). Once diagnosed, children with SCID receive prolonged courses of antibiotics and breast-feeding frequently ceases during this critical time for gut microbiome development.3Chemotherapeutic conditioning often precedes HSCT and can cause mucositis and severe immunosuppression, increasing the risk of bacteremia. HSCT can be complicated by graft-versus-host-disease (GvHD) causing severe gut inflammation. In HSCT in adults, overgrowth by a dominant gut microbiome species and the subsequent reduced diversity have been associated with gut GvHD4, 5and bacteremia.6However, the gut microbiome in HSCT in infancy, specifically in SCID, has not been explored.",

author = "Lane, {Jonathan P.} and Christopher Stewart and Stephen Cummings and Gennery, {Andrew R.}",

year = "2015",

month = mar,

day = "12",

doi = "10.1016/j.jaci.2015.01.024",

language = "English",

volume = "135",

pages = "1654--1656",

journal = "Journal of Allergy and Clinical Immunology",

issn = "0091-6749",

publisher = "Mosby Inc.",

number = "6",

}

TY - JOUR

T1 - Gut microbiome variations during hematopoietic stem cell transplant in severe combined immunodeficiency.

AU - Lane, Jonathan P.

AU - Stewart, Christopher

AU - Cummings, Stephen

AU - Gennery, Andrew R.

PY - 2015/3/12

Y1 - 2015/3/12

N2 - The composition of the gut microbiome is unstable in infancy,1with many environmental factors determining its development including mode of delivery, method of feeding, antibiotic exposure, and neonatal hospitalisation.2Severe combined immunodeficiency (SCID), a primary T-lymphocyte immunodeficiency causing severe viral infections, Pneumocystis jiroveci pneumonitis, chronic diarrhea, and failure to thrive, is fatal in infancy without hematopoietic stem cell transplantation (HSCT). Once diagnosed, children with SCID receive prolonged courses of antibiotics and breast-feeding frequently ceases during this critical time for gut microbiome development.3Chemotherapeutic conditioning often precedes HSCT and can cause mucositis and severe immunosuppression, increasing the risk of bacteremia. HSCT can be complicated by graft-versus-host-disease (GvHD) causing severe gut inflammation. In HSCT in adults, overgrowth by a dominant gut microbiome species and the subsequent reduced diversity have been associated with gut GvHD4, 5and bacteremia.6However, the gut microbiome in HSCT in infancy, specifically in SCID, has not been explored.

AB - The composition of the gut microbiome is unstable in infancy,1with many environmental factors determining its development including mode of delivery, method of feeding, antibiotic exposure, and neonatal hospitalisation.2Severe combined immunodeficiency (SCID), a primary T-lymphocyte immunodeficiency causing severe viral infections, Pneumocystis jiroveci pneumonitis, chronic diarrhea, and failure to thrive, is fatal in infancy without hematopoietic stem cell transplantation (HSCT). Once diagnosed, children with SCID receive prolonged courses of antibiotics and breast-feeding frequently ceases during this critical time for gut microbiome development.3Chemotherapeutic conditioning often precedes HSCT and can cause mucositis and severe immunosuppression, increasing the risk of bacteremia. HSCT can be complicated by graft-versus-host-disease (GvHD) causing severe gut inflammation. In HSCT in adults, overgrowth by a dominant gut microbiome species and the subsequent reduced diversity have been associated with gut GvHD4, 5and bacteremia.6However, the gut microbiome in HSCT in infancy, specifically in SCID, has not been explored.

U2 - 10.1016/j.jaci.2015.01.024

DO - 10.1016/j.jaci.2015.01.024

M3 - Article

VL - 135

SP - 1654

EP - 1656

JO - Journal of Allergy and Clinical Immunology

JF - Journal of Allergy and Clinical Immunology

SN - 0091-6749

IS - 6

ER -