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List of works by Frédéric Rieux-Laucat

A Mendelian predisposition to B-cell lymphoma caused by IL-10R deficiency

scientific article published on 2 October 2013

A new peak in the ALPS

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

scientific article (publication date: 3 November 2011)

Accessory spleen: Differential diagnosis for lymphoma in autoimmune lymphoproliferative syndrome

Activation-induced cytidine deaminase (AID) is required for B-cell tolerance in humans

scientific article

Anomalies d’expression du complexe récepteur T de l’antigène/CD3 et déficits immunitaires

scientific article published on 01 February 2007

Are RASopathies new monogenic predisposing conditions to the development of systemic lupus erythematosus? Case report and systematic review of the literature

scientific article published on 17 June 2013

Around the V(D)J recombinase machinery.

scientific article published on February 1994

Atypical Manifestation of LPS-Responsive Beige-Like Anchor Deficiency Syndrome as an Autoimmune Endocrine Disorder without Enteropathy and Immunodeficiency

scientific article

Auto-antibodies against type I IFNs in patients with life-threatening COVID-19

scientific article published on 24 September 2020

Autoimmune Lymphoproliferative Syndrome and Perforin

scientific article published on 01 January 2005

Autoimmune Lymphoproliferative Syndrome-FAS Patients Have an Abnormal Regulatory T Cell (Treg) Phenotype but Display Normal Natural Treg-Suppressive Function on T Cell Proliferation.

scientific article published on 9 April 2018

Autoimmune lymphoproliferative syndrome (ALPS). Case report and family history.

scientific article

Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation

scientific article published on 31 July 2012

Autoimmune lymphoproliferative syndrome with somatic Fas mutations

scientific article

Autoimmune lymphoproliferative syndrome: a multifactorial disorder ⬇️

scientific article published on November 1, 2010

Autoimmune lymphoproliferative syndromes (ALPS): models for the study of peripheral tolerance.

scientific article

CD2-induced apoptosis in activated human peripheral T cells: a Fas-independent pathway that requires early protein tyrosine phosphorylation

scientific article published on 01 May 1996

CD34-positive early human thymocytes: T cell receptor and cytokine receptor gene expression

article

Cell-death signaling and human disease

scientific article

Characterization of antigen-specific repertoire diversity following in vitro restimulation by a recombinant adenovirus expressing human cytomegalovirus pp65.

scientific article published on March 2003

Childhood linear IgA disease in association with autoimmune lymphoproliferative syndrome

scientific article published in March 2004

Clinical and molecular aspects of autoimmune enteropathy and immune dysregulation, polyendocrinopathy autoimmune enteropathy X-linked syndrome

scientific article

Clinical effects of mutations to CD95 (Fas): relevance to autoimmunity?

scientific article published on January 1998

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study ⬇️

scientific article published on 16 July 2016

Clinical, immunological, and pathological consequences of Fas-deficient conditions

scientific article published in September 1996

Combined immunodeficiency associated with increased apoptosis of lymphocytes and radiosensitivity fibroblasts

scientific article published on 01 July 1999

Correction of Fas (CD95) deficiency by haploidentical bone marrow transplantation.

scientific article

Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome

scientific article published on 15 September 2008

Cytomegalovirus infection in infants with autoimmune lymphoproliferative syndrome (ALPS)

Defective IL10 signaling defining a subgroup of patients with inflammatory bowel disease.

scientific article published on 26 April 2011

Defective anti-polysaccharide response and splenic marginal zone disorganization in ALPS patients

scientific article published on 26 June 2014

Defective human interleukin 2 receptor gamma chain in an atypical X chromosome-linked severe combined immunodeficiency with peripheral T cells

scientific article

Deficiency in Mucosa-associated Lymphoid Tissue Lymphoma Translocation 1: A Novel Cause of IPEX-Like Syndrome

scientific article

Detection of interferon alpha protein reveals differential levels and cellular sources in disease.

scientific article published on 18 April 2017

Diagnosis of autoimmune lymphoproliferative syndrome caused by FAS deficiency in adults

scientific article published on 14 September 2012

Differential sensitivity of Jurkat and primary T cells to caspase-independent cell death triggered upon Fas stimulation

scientific article published on 01 August 2002

Diffuse large B-cell non-Hodgkin's lymphoma in a patient with autoimmune lymphoproliferative syndrome

scientific article published on 01 May 2001

Digestive histopathological presentation of IPEX syndrome

Disease-associated mutations identify a novel region in human STING necessary for the control of type I interferon signaling

scientific article published on 3 January 2017

Distinct systemic and mucosal immune responses during acute SARS-CoV-2 infection

scientific article published on 01 September 2021

Dyserythropoiesis associated with a Fas-deficient condition in childhood

scientific article published on 01 February 2000

Early-onset autoimmunity associated with SOCS1 haploinsufficiency

scientific article published on 21 October 2020

Early-onset hypogammaglobulinemia: A survey of 44 patients

scientific article published on 08 May 2015

Efficacy of gene therapy for X-linked severe combined immunodeficiency

scientific article

Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment of vasculopathy associated with TMEM173-activating mutations in 3 children.

scientific article published on 20 August 2016

Evans Syndrome in Children: Long-Term Outcome in a Prospective French National Observational Cohort

scientific article

Evolution of disease activity and biomarkers on and off rapamycin in 28 patients with autoimmune lymphoproliferative syndrome

scientific article published on 27 October 2016

Expression of Granzyme B in viral hepatitis in patients with ALPS.

scientific article published in March 2004

Expression of the HLA-C2-specific activating killer-cell Ig-like receptor KIR2DS1 on NK and T cells

scientific article

FAS and RAS related Apoptosis defects: From autoimmunity to leukemia

scientific article published on 01 January 2019

FAS-L, IL-10, and double-negative CD4- CD8- TCR alpha/beta+ T cells are reliable markers of autoimmune lymphoproliferative syndrome (ALPS) associated with FAS loss of function

scientific article

FAS/FAS-L dependent killing of activated human monocytes and macrophages by CD4+CD25- responder T cells, but not CD4+CD25+ regulatory T cells

scientific article published on 24 December 2011

Failure of HY-Specific Thymocytes to Escape Negative Selection by Receptor Editing

article

Familial and syndromic lupus share the same phenotype as other early-onset forms of lupus

scientific article published on 27 December 2016

Germline TET2 Loss-Of-Function Causes Childhood Immunodeficiency And Lymphoma

scientific article published on 09 June 2020

Gray platelet syndrome can mimic autoimmune lymphoproliferative syndrome

scientific article published in October 2015

Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome

scientific article

Human TCR alpha/beta+ CD4-CD8- double-negative T cells in patients with autoimmune lymphoproliferative syndrome express restricted Vbeta TCR diversity and are clonally related to CD8+ T cells

scientific article published on July 2008

Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness

scientific article

Hypomorphic mutation of ZAP70 in human results in a late onset immunodeficiency and no autoimmunity.

scientific article published in July 2009

Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency

scientific article

Immunologic evaluation and genetic defects of apoptosis in patients with autoimmune lymphoproliferative syndrome (ALPS)

scientific article published on 23 December 2020

Immunology. Autoimmunity by haploinsufficiency

scientific article published on September 2014

Impaired type I interferon activity and inflammatory responses in severe COVID-19 patients

scientific article published on 13 July 2020

In Vitro Evaluation of the Apoptosis Function in Human Activated T Cells

Inactivation of the Fas gene by Alu insertion: retrotransposition in an intron causing splicing variation and autoimmune lymphoproliferative syndrome.

scientific article published in October 2002

Induction of T lymphocyte apoptosis by sulphasalazine in patients with Crohn's disease.

scientific article published on November 2004

Inherited Immunodeficiency: A New Association With Early-Onset Childhood Panniculitis

scientific article published in April 2018

Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations ⬇️

scientific article

Inherited and acquired death receptor defects in human Autoimmune Lymphoproliferative Syndrome

scientific article

Inherited and somatic CD3zeta mutations in a patient with T-cell deficiency

article published in 2006

Intrinsic antiproliferative activity of the innate sensor STING in T lymphocytes

scientific article

Investigation of common variable immunodeficiency patients and healthy individuals using autoimmune lymphoproliferative syndrome biomarkers

scientific article published on 28 August 2013

LRBA deficiency with autoimmunity and early onset chronic erosive polyarthritis

scientific article

Lack of selective V beta deletion in peripheral CD4+ T cells of human immunodeficiency virus-infected infants

scientific article published in August 1993

Le lupus systémique à début pédiatrique : une pathologie polygénique ou monogénique ?

scientific article published on 26 November 2012

Le modèle dutwo-hitde Knudson s’applique aux maladies auto-immunes ⬇️

scientific article published on January 1, 2011

Le syndrome lymphoprolifératif avec auto-immunité : un défaut hérité ou acquis d’apoptose lymphocytaire

Live and let die at TEMRA.

scientific article published on August 2014

Long-term follow up of IPEX syndrome patients after different therapeutic strategies: an international multicenter retrospective study.

scientific article published on 11 December 2017

Long-term immune reconstitution in RAG-1-deficient mice treated by retroviral gene therapy: a balance between efficiency and toxicity

scientific article

Lymphoproliferative syndrome with autoimmunity: A possible genetic basis for dominant expression of the clinical manifestations

scientific article published on 01 October 1999

MHC-restricted T cell receptor signaling is required for αβ TCR replacement of the pre T cell receptor

scientific article published on 01 February 2008

MST1 mutations in autosomal recessive primary immunodeficiency characterized by defective naive T-cell survival

scientific article published on 14 December 2011

Mycophenolate mofetil as an alternate immunosuppressor for autoimmune lymphoproliferative syndrome.

scientific article

Naturally occurring primary deficiencies of the immune system

scientific article published on January 1997

Normal T cell receptor Vβ usage in a primary immunodeficiency associated with HLA class II deficiency

scientific article published on 01 April 1993

ORAI1 mutations abolishing store-operated Ca2+ entry cause anhidrotic ectodermal dysplasia with immunodeficiency

scientific article published on 15 November 2017

Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation

scientific article

Overexpression of the antiapoptotic gene Bfl-1 in B cells from patients with familial systemic lupus erythematosus

article

PReS-FINAL-2353: Are rasopathies new monogenic predisposing conditions to the development of systemic lupus erythematosus?

scientific article published on 5 December 2013

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations

scientific article published on 9 January 2018

Perforin-dependent apoptosis functionally compensates Fas deficiency in activation-induced cell death of human T lymphocytes

scientific article published on 27 August 2007

Phenotypic characterization of very early-onset IBD due to mutations in the IL10, IL10 receptor alpha or beta gene: a survey of the Genius Working Group

scientific article published on December 2013

Primary T-cell immunodeficiency with immunodysregulation caused by autosomal recessive LCK deficiency.

scientific article

RAS-associated lymphoproliferative disease evolves into severe juvenile myelo-monocytic leukemia

scientific article published in March 2014

Reduced expression of FOXP3 and regulatory T-cell function in severe forms of early-onset autoimmune enteropathy

scientific article published on 9 June 2010

Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop

scientific article

STIM1 mutation associated with a syndrome of immunodeficiency and autoimmunity

scientific article

Severe Pulmonary Fibrosis as the First Manifestation of Interferonopathy (TMEM173 Mutation).

scientific article published in September 2016

Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene

scientific article

Significance of Interdigitating Reticulum Cells in Omenn's Syndrome

scientific article published on 01 August 1996

Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4<sup>+</sup> T cell perturbations

scientific article published on 08 April 2021

Somatic loss of heterozygosity, but not haploinsufficiency alone, leads to full-blown autoimmune lymphoproliferative syndrome in 1 of 12 family members with FAS start codon mutation

Stimulator of Interferon Genes-Associated Vasculopathy With Onset in Infancy: A Mimic of Childhood Granulomatosis With Polyangiitis

scientific article published on 20 May 2015

T cell activation deficiencies.

scientific article published on September 1995

The Autoimmune Lymphoproliferative Syndrome with Defective FAS or FAS-Ligand Functions

scholarly article by Frédéric Rieux-Laucat et al published 17 June 2018 in Journal of Clinical Immunology

Type I interferon-mediated autoinflammation due to DNase II deficiency

scientific article published on 19 December 2017

VPS33B regulates protein sorting into and maturation of α-granule progenitor organelles in mouse megakaryocytes

scientific journal article

What's up in the ALPS.

scientific article published on 23 October 2017

Whole-exome-sequencing-based discovery of human FADD deficiency

scientific article

X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) gene

scientific journal article

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome

scientific article

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