Neutrophilic dermatoses and autoinflammatory diseases with skin involvement—innate immune disorders

Anakinra Improves Pyoderma Gangrenosum in Psoriatic Arthritis: A Case Report

(2015) Marie Acquitter et al.   ANNALS OF INTERNAL MEDICINE

Molecular Mechanisms in Genetically Defined Autoinflammatory Diseases: Disorders of Amplified Danger Signaling

(2015) Adriana Almeida de Jesus et al.   Annual Review of Immunology

The genetics of pyoderma gangrenosum and implications for treatment: a systematic review

(2015) E.M. DeFilippis et al.   BRITISH JOURNAL OF DERMATOLOGY

Canakinumab in adults with steroid-refractory pyoderma gangrenosum

(2015) A.G.A. Kolios et al.   BRITISH JOURNAL OF DERMATOLOGY

Severe Sweet's Syndrome with Elevated Cutaneous Interleukin-1β after Azathioprine Exposure: Case Report and Review of the Literature

(2015) Laurence Imhof et al.   DERMATOLOGY

Myeloid lineage–restricted somatic mosaicism of NLRP3 mutations in patients with variant Schnitzler syndrome

(2015) Heleen D. de Koning et al.   JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY

Sweet's Syndrome in Patients with MDS and MEFV Mutations

(2015) Tatsuro Jo et al.   NEW ENGLAND JOURNAL OF MEDICINE

New monogenic autoinflammatory diseases—a clinical overview

(2015) Scott W. Canna et al.   Seminars in Immunopathology

AP1S3 Mutations Are Associated with Pustular Psoriasis and Impaired Toll-like Receptor 3 Trafficking

(2014) Niovi Setta-Kaffetzi et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)

(2014) P. K. Chakraborty et al.   BLOOD

Expression of cytokines, chemokines and other effector molecules in two prototypic autoinflammatory skin diseases, pyoderma gangrenosum and Sweet's syndrome

(2014) A. V. Marzano et al.   CLINICAL AND EXPERIMENTAL IMMUNOLOGY

An inherited mutation inNLRC4causes autoinflammation in human and mice

(2014) Akiko Kitamura et al.   JOURNAL OF EXPERIMENTAL MEDICINE

Expression of interleukin-1 alpha in amicrobial pustulosis of the skin folds with complete response to anakinra

(2014) Emmanuelle Amazan et al.   JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY

Erythema elevatum diutinum: a review of presentation and treatment

(2014) S.E. Momen et al.   JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2

(2014) Qing Zhou et al.   NEW ENGLAND JOURNAL OF MEDICINE

Activated STING in a Vascular and Pulmonary Syndrome

(2014) Yin Liu et al.   NEW ENGLAND JOURNAL OF MEDICINE

Schnitzler’s syndrome: lessons from 281 cases

(2014) Heleen D de Koning   Clinical and Translational Allergy

A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD)

(2013) D. H. Wiseman et al.   BLOOD

X-linked inhibitor of apoptosis (XIAP) deficiency: The spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosis

(2013) C. Speckmann et al.   CLINICAL IMMUNOLOGY

Autoinflammatory Skin Disorders in Inflammatory Bowel Diseases, Pyoderma Gangrenosum and Sweet’s Syndrome: a Comprehensive Review and Disease Classification Criteria

(2013) Angelo V. Marzano et al.   CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY

Neutrophilic dermatoses as systemic diseases

(2013) Lola Prat et al.   CLINICS IN DERMATOLOGY

Autoinflammatory Pustular Neutrophilic Diseases

(2013) Haley B. Naik et al.   DERMATOLOGIC CLINICS

Systemic lupus erythematosus–associated neutrophilic dermatosis—an underrecognized neutrophilic dermatosis in patients with systemic lupus erythematosus

(2013) Allison R. Larson et al.   HUMAN PATHOLOGY

Sweet syndrome: Clinical presentation, associations, and response to treatment in 77 patients

(2013) Nicole M. Rochet et al.   JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY

Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis

(2012) Catherine T. Jordan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A Hypermorphic Missense Mutation in PLCG2 , Encoding Phospholipase Cγ2, Causes a Dominantly Inherited Autoinflammatory Disease with Immunodeficiency

(2012) Qing Zhou et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Sustained response and prevention of damage progression in patients with neonatal-onset multisystem inflammatory disease treated with anakinra: A cohort study to determine three- and five-year outcomes

(2012) Cailin H. Sibley et al.   ARTHRITIS AND RHEUMATISM

Acute febrile neutrophilic dermatosis (Sweetʼs syndrome)

(2012) Charles L. Anzalone et al.   CURRENT OPINION IN HEMATOLOGY

Sweet's syndrome with subcutaneous involvement associated with pegfilgrastim treatment: first reported case

(2012) Mar Llamas-Velasco et al.   JOURNAL OF CUTANEOUS PATHOLOGY

Mutations in IL36RN/IL1F5 Are Associated with the Severe Episodic Inflammatory Skin Disease Known as Generalized Pustular Psoriasis

(2011) Alexandros Onoufriadis et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Alteration in the Gene Encoding Protein Tyrosine Phosphatase Nonreceptor Type 6 (PTPN6/SHP1) May Contribute to Neutrophilic Dermatoses

(2011) Andrew B. Nesterovitch et al.   AMERICAN JOURNAL OF PATHOLOGY

A novel mutation of IL1RN in the deficiency of interleukin-1 receptor antagonist syndrome: Description of two unrelated cases from Brazil

(2011) Adriana A. Jesus et al.   ARTHRITIS AND RHEUMATISM

High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: Results of an international multicenter collaborative study

(2011) Naoko Tanaka et al.   ARTHRITIS AND RHEUMATISM

Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity

(2011) Yin Liu et al.   ARTHRITIS AND RHEUMATISM

A mutation in the immunoproteasome subunit PSMB8 causes autoinflammation and lipodystrophy in humans

(2011) Akiko Kitamura et al.   JOURNAL OF CLINICAL INVESTIGATION

Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature

(2011) Tracy A Briggs et al.   NATURE GENETICS

Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity

(2011) Ekkehart Lausch et al.   NATURE GENETICS

Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis

(2011) Slaheddine Marrakchi et al.   NEW ENGLAND JOURNAL OF MEDICINE

Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome

(2010) Georgia Ramantani et al.   ARTHRITIS AND RHEUMATISM

Role of inflammatory cells, cytokines and matrix metalloproteinases in neutrophil-mediated skin diseases

(2010) A. V. Marzano et al.   CLINICAL AND EXPERIMENTAL IMMUNOLOGY

Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome

(2010) Antonio Torrelo et al.   JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY

Horror Autoinflammaticus: The Molecular Pathophysiology of Autoinflammatory Disease

(2009) Seth L. Masters et al.   Annual Review of Immunology

Targeted treatment of pyoderma gangrenosum in PAPA (pyogenic arthritis, pyoderma gangrenosum and acne) syndrome with the recombinant human interleukin-1 receptor antagonist anakinra

(2009) M. Brenner et al.   BRITISH JOURNAL OF DERMATOLOGY

Sweet’s syndrome in familial Mediterranean fever: possible continuum of the neutrophilic reaction as a new cutaneous feature of FMF

(2009) Tugba Oskay et al.   JOURNAL OF CUTANEOUS PATHOLOGY

Fresh from the biologic pipeline

(2009) Randall Osborne   NATURE BIOTECHNOLOGY

An Autoinflammatory Disease with Deficiency of the Interleukin-1–Receptor Antagonist

(2009) Ivona Aksentijevich et al.   NEW ENGLAND JOURNAL OF MEDICINE

Familial Mediterranean Fever Gene as a Possible Modifier of Sweet Syndrome with Chronic Myelogenous Leukemia

(2008) Takashi Miyoshi et al.   ACTA HAEMATOLOGICA

HMG-CoA reductase inhibition induces IL-1  release through Rac1/PI3K/PKB-dependent caspase-1 activation

(2008) L. M. Kuijk et al.   BLOOD

Pyoderma gangrenosum associated with subcorneal pustular dermatosis and IgA myeloma

(2008) K. Ahmad et al.   CLINICAL AND EXPERIMENTAL DERMATOLOGY