Unrelated partially matched lymphocyte infusions in a patient with complete DiGeorge/CHARGE syndrome
Language English Country Denmark Media print
Document type Case Reports, Journal Article, Research Support, Non-U.S. Gov't
PubMed
17493228
DOI
10.1111/j.1399-3046.2007.00702.x
PII: PTR702
Knihovny.cz E-resources
- MeSH
- Anus, Imperforate therapy MeSH
- DiGeorge Syndrome blood therapy MeSH
- Coloboma therapy MeSH
- Humans MeSH
- Intellectual Disability therapy MeSH
- Genitalia, Male abnormalities MeSH
- Follow-Up Studies MeSH
- Graft vs Host Disease etiology prevention & control MeSH
- Ear Diseases congenital therapy MeSH
- Infant, Newborn MeSH
- Growth Disorders therapy MeSH
- T-Lymphocytes MeSH
- Lymphocyte Transfusion adverse effects methods MeSH
- Ear abnormalities MeSH
- Heart Defects, Congenital therapy MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Infant, Newborn MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Research Support, Non-U.S. Gov't MeSH
We present an infant with cDGS overlapping with CHARGE syndrome, who suffered from T-cell deficiency treated with screened healthy DLI from an unrelated donor (8/10 match). The first dose of DLI (1.1 x 10(6) CD3+/kg) was administered at the age of six months, the second one (0.9 x 10(6) CD3+/kg) 36 days later. No conditioning was employed, GvHD prophylaxis consisting of CsA was used only during the second infusion. Since day+10 after the first DLI, split chimerism showing T-cell engraftment has been documented. Proliferative response to PHA was detected on day+145. The treatment was complicated by severe acute GvHD (grade II-III) after the first DLI and prolonged chronic liver cholestatic GvHD developing after the second DLI. Vigorous EBV proliferation four wk after the second DLI was accompanied by peripheral expansion of CD8+ donor cells. The patient, 26-months old, is clinically well and has slowly started to gain his developmental milestones. We believe that infusions of small doses of DLI from an unrelated donor represent a potentially helpful therapeutic option in patients with cDGS/CHARGE phenotype.
References provided by Crossref.org
Beyond TREC: Pivotal role of tandem TREC/KREC assay in Czech SCID NBS pilot programme
The TREC/KREC assay for the diagnosis and monitoring of patients with DiGeorge syndrome
Helios expression in T-regulatory cells in patients with di George Syndrome