Isabel Moreno Hernández

ORCID: 0000-0001-5280-2302
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Research Areas
  • Psoriasis: Treatment and Pathogenesis
  • vaccines and immunoinformatics approaches
  • Immunotherapy and Immune Responses
  • Gastrointestinal motility and disorders
  • Chronic Obstructive Pulmonary Disease (COPD) Research
  • Autoimmune Bullous Skin Diseases
  • Congenital gastrointestinal and neural anomalies
  • Systemic Lupus Erythematosus Research
  • Monoclonal and Polyclonal Antibodies Research
  • Pediatric health and respiratory diseases
  • Cancer and Skin Lesions
  • Rheumatoid Arthritis Research and Therapies
  • Restraint-Related Deaths
  • Parasitic Diseases Research and Treatment
  • Nursing care and research
  • Salivary Gland Tumors Diagnosis and Treatment
  • Hemoglobinopathies and Related Disorders
  • Entomological Studies and Ecology
  • Breast Lesions and Carcinomas
  • Spondyloarthritis Studies and Treatments
  • Parvovirus B19 Infection Studies
  • Anorectal Disease Treatments and Outcomes
  • Spinal Dysraphism and Malformations
  • Dermatology and Skin Diseases
  • Skin and Cellular Biology Research

Hospital Arnau de Vilanova
2019-2021

Hospital de Sagunto
2014

Hospital Oncológico Docente "Conrado Benítez García"
2013

Hospital de Mataró
2007-2009

Induction of immune tolerance as therapeutic approach for autoimmune diseases constitutes a current research focal point. In this sense, we aimed to evaluate an altered peptide ligand (APL) induction peripheral in patients with rheumatoid arthritis (RA). A novel T-cell epitope from human heat-shock protein 60 (Hsp60), autoantigen involved the pathogenesis RA, was identified by bioinformatics tools and APL design starting epitope. We investigated ability inducing regulatory T cells (Treg...

10.3109/08916934.2010.550590 article EN Autoimmunity 2011-03-03

T cells are involved in the pathogenesis of rheumatoid arthritis (RA). CD6 is a co-stimulatory molecule, predominantly expressed on lymphocytes, that has been linked to autoreactive responses. The purpose this study was evaluate safety, immunogenicity and preliminary efficacy itolizumab, humanized anti-CD6 monoclonal antibody, patients with active arthritis. Fifteen were enrolled phase I, open-label, dose-finding study. Five cohorts received weekly antibody monotherapy dose-range from 0.1...

10.1016/j.rinim.2012.11.001 article EN cc-by-nc-nd Results in Immunology 2012-01-01

Summary Itolizumab is a humanized anti-CD6 monoclonal antibody (mAb) that has previously shown encouraging results, in terms of safety and positive clinical effects, 6-week monotherapy trial conducted rheumatoid arthritis (RA) patients. The current Phase I study evaluated the response for longer treatment 12 itolizumab intravenous doses subjects with active RA despite previous disease-modifying anti-rheumatic drug (DMARD) therapy. Twenty-one were enrolled into four dosage groups (0·1, 0·2,...

10.1111/cei.13061 article EN Clinical & Experimental Immunology 2017-09-30

Rheumatoid arthritis is a systemic autoimmune disease mediated by T cells. Productive engagement of cell receptors major histocompatibility complex-peptide leads to proliferation, differentiation and the definition effector functions. Altered peptide ligands (APL) generated amino acid substitutions in antigenic have diverse effects on response. We predicted novel epitope from human heat-shock protein 60, an autoantigen involved pathogenesis rheumatoid arthritis. Three APLs were designed this...

10.3109/08916934.2012.697592 article EN Autoimmunity 2012-06-11

10.1016/s1134-2072(13)70639-x article LT FMC - Formación Médica Continuada en Atención Primaria 2013-10-01

10.1016/s1134-2072(15)70890-x article FR FMC - Formación Médica Continuada en Atención Primaria 2015-01-01

Objectives: To report a case of response to ustekinumab in patient with severe psoriasis when adalimumab dose escalation fail.Case Description: A 35-year-old Caucasian male was diagnosed as having psoriasis. He started on methotrexate followed cyclosporine. Despite these treatments, the experienced an abrupt deterioration his [PASI 35]. The treatment adalimumab: initial 80mg by 40mg week 2. At 3 he continued 40mg/two weeks significant reduction After 8 months therapy, referred that effective...

10.6000/1927-5951.2014.04.02.9 article EN cc-by-nc Journal of Pharmacy and Nutrition Sciences 2014-04-30

10.1016/j.fmc.2014.07.006 article IT FMC - Formación Médica Continuada en Atención Primaria 2016-01-01

10.1016/j.fmc.2015.09.009 article ES FMC - Formación Médica Continuada en Atención Primaria 2016-03-01

10.1016/j.fmc.2014.07.009 article FMC - Formación Médica Continuada en Atención Primaria 2016-02-01

10.1016/j.fmc.2014.03.008 article ES FMC - Formación Médica Continuada en Atención Primaria 2015-10-01

10.1016/s1134-2072(13)70549-8 article FR FMC - Formación Médica Continuada en Atención Primaria 2013-03-01

10.1016/s1134-2072(11)70140-2 article ES FMC - Formación Médica Continuada en Atención Primaria 2011-06-01

10.1016/s1134-2072(13)70622-4 article FMC - Formación Médica Continuada en Atención Primaria 2013-08-01

10.1016/s1134-2072(09)71270-8 article ES FMC - Formación Médica Continuada en Atención Primaria 2009-05-01

10.1016/s1134-2072(10)70120-1 article FMC - Formación Médica Continuada en Atención Primaria 2010-05-01

10.1016/s1134-2072(10)70011-6 article FMC - Formación Médica Continuada en Atención Primaria 2010-01-01

10.1016/s1134-2072(07)71906-0 article FMC - Formación Médica Continuada en Atención Primaria 2007-11-01

10.1016/j.fmc.2016.02.014 article ES FMC - Formación Médica Continuada en Atención Primaria 2017-05-01

10.1016/s1134-2072(07)71573-6 article NL FMC - Formación Médica Continuada en Atención Primaria 2007-03-01

10.1016/s1134-2072(07)71949-7 article IT FMC - Formación Médica Continuada en Atención Primaria 2007-12-01

10.1016/s1134-2072(07)71603-1 article IT FMC - Formación Médica Continuada en Atención Primaria 2007-04-01
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