|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
In western countries, X-linked interleukin 2 receptor gamma chain (IL2RG) and adenosine deaminase (ADA) deficiency SCID are two of the most common types of SCID and can be treated by GT.
|
31024866 |
2019 |
|
Severe Combined Immunodeficiency
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Inherited defects in adenosine deaminase (ADA) cause a subtype of severe combined immunodeficiency (SCID) known as severe combined immune deficiency caused by adenosine deaminase defects (ADA-SCID).
|
30194989 |
2019 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
Human adenosine deaminase 1 deficiency was described in the 1970s to cause severe combined immunodeficiency.
|
30565235 |
2019 |
|
Severe Combined Immunodeficiency
|
0.500 |
AlteredExpression
|
disease |
BEFREE |
Although ADA enzymatic levels were suggestive of ADA-SCID, the child did not present the classical signs of ADA deficiency; therefore, the initial diagnosis was of a conventional SCID.
|
29355610 |
2018 |
|
Severe Combined Immunodeficiency
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
We describe a case of an infant diagnosed with severe combined immune deficiency (Adenosine Deaminase (ADA), SCID) with severe retinopathy and associated low vision in both eyes at first examination.
|
28812413 |
2018 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
Survival, infections, systemic sequelae, and laboratory assessments were recorded for all ADA-deficient SCID patients, managed at a single center since 1985, who survived 5 or more years following treatment.
|
28748310 |
2017 |
|
Severe Combined Immunodeficiency
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Adenosine Deaminase (ADA) deficiency is an autosomal recessive variant of severe combined immunodeficiency (SCID) caused by systemic accumulation of ADA substrates.
|
28074903 |
2017 |
|
Severe Combined Immunodeficiency
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Severe combined immunodeficiency (SCID) is a potentially fatal primary immunodeficiency (PID) that is caused by mutations in genes such as IL2RG, JAK3, IL7RA, RAG1, RAG2, and ADA.
|
28552805 |
2017 |
|
Severe Combined Immunodeficiency
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
Twenty-five years have passed since first attempts of gene therapy (GT) in children affected by severe combined immunodeficiency (SCID) due to adenosine deaminase (ADA) defect, also known by the general public as bubble babies.
|
28847159 |
2017 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
Adenosine Deaminase (ADA)-Deficient Severe Combined Immune Deficiency (SCID): Molecular Pathogenesis and Clinical Manifestations.
|
28842866 |
2017 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
Adenosine deaminase (ADA) deficiency is a rare, autosomal-recessive systemic metabolic disease characterized by severe combined immunodeficiency (SCID).
|
27129325 |
2016 |
|
Severe Combined Immunodeficiency
|
0.500 |
GeneticVariation
|
disease |
BEFREE |
The xenograft model used is not informative for adenosine deaminase-SCID, whereas hypomorphic mutations lead to less severe arrests in development.
|
26441229 |
2016 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
We carried out a retrospective analysis of the ADA gene in 46 known ADA deficient SCID patients on whom DNA had been stored.
|
26255240 |
2015 |
|
Severe Combined Immunodeficiency
|
0.500 |
AlteredExpression
|
disease |
BEFREE |
ADA is ubiquitously expressed in all tissues of the body but most profoundly affects lymphocyte development and function leading to severe combined immunodeficiency (SCID).
|
25875700 |
2015 |
|
Severe Combined Immunodeficiency
|
0.500 |
AlteredExpression
|
disease |
BEFREE |
These results suggest that this approach can be scaled-up to clinical levels for treatment of ADA-deficient severe combined immune deficiency subjects with suboptimal hematopoietic stem cell transplantation options.
|
24925206 |
2014 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
Gene transfer into autologous hematopoietic stem cells by γ-retroviral vectors (gRV) is an effective treatment for adenosine deaminase (ADA)-deficient severe combined immunodeficiency (SCID).
|
24256635 |
2014 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
This review details gene therapy trials for X-linked and adenosine deaminase (ADA)-deficient severe combined immunodeficiency (SCID), Wiskott-Aldrich syndrome (WAS) and chronic granulomatous disease (CGD).
|
24848753 |
2014 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
The development of autologous hematopoietic stem cell gene therapy provides another treatment of the X-linked and adenosine deaminase-deficient forms of SCID, and we discuss how we have integrated gene therapy into our treatment strategy.
|
24113871 |
2013 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
Adenosine deaminase (ADA)-severe combined immunodeficiency (SCID) is caused by genetic variants that disrupt the function of ADA.
|
23280131 |
2013 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase-deficient severe combined immune deficiency.
|
22153773 |
2012 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
These studies directly demonstrate the importance of providing nonmyeloablative pretransplantation conditioning to achieve therapeutic benefits with gene therapy for ADA-deficient severe combined immunodeficiency.
|
22968453 |
2012 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
We report a child with severe combined immunodeficiency (T-B- SCID) due to ADA deficiency diagnosed at the age of 1 month, whose lymphocyte counts including CD4+ and CD8+ T and NK cells began to improve after several months with normalization of ADA activity in Peripheral blood lymphocytes (PBL), as a result of somatic mosaicism caused by monoallelic reversion of the causative mutation in the ADA gene.
|
21671975 |
2011 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
Myeloid dysplasia and bone marrow hypocellularity in adenosine deaminase-deficient severe combined immune deficiency.
|
21725047 |
2011 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
Furthermore, numerous trials using similar gene vectors to transfer genes into mature T cells have not been complicated by clonal outgrowth.This explains the great interest ina deeper understanding of retroviral vector–host interactions in the therapeutic setting of SCID-ADA.
|
21254403 |
2011 |
|
Severe Combined Immunodeficiency
|
0.500 |
Biomarker
|
disease |
BEFREE |
We studied these issues in patients affected by adenosine deaminase severe combined immune deficiency after low-intensity conditioning and reinfusion of retrovirally transduced autologous CD34(+) cells.
|
21477850 |
2011 |