Literature DB >> 12190932

Primary immunodeficiency diseases: dissectors of the immune system.

Rebecca H Buckley1.   

Abstract

The past 50 years have seen enormous progress in this field. An unknown concept until 1952, there are now more than 100 different primary immunodeficiency syndromes in the world's literature. Each novel syndrome has shed new insight into the workings of the immune system, dissecting its multiple parts into unique functioning components. This has been especially true over the past decade, as the molecular bases of approximately 40 of these diseases have been identified in rapid succession. Advances in the treatment of these diseases have also been impressive. Antibody replacement has been improved greatly by the development of human immunoglobulin preparations that can be safely administered by the intravenous route, and cytokine and humanized anticytokine therapies are now possible through recombinant technologies. The ability to achieve life-saving immune reconstitution of patients with lethal severe combined immunodeficiency by administering rigorously T-cell-depleted allogeneic related haploidentical bone marrow stem cells has extended this option to virtually all such infants, if diagnosed before untreatable infections develop. Finally, the past 3 years have witnessed the first truly successful gene therapy. The impressive results in X-linked severe combined immunodeficiency offer hope that this approach can be extended to many more diseases in the future.

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Year:  2002        PMID: 12190932     DOI: 10.1034/j.1600-065x.2002.18517.x

Source DB:  PubMed          Journal:  Immunol Rev        ISSN: 0105-2896            Impact factor:   12.988


  19 in total

1.  Peripheral T-cell lymphoma and Job's syndrome: a rare association.

Authors:  Ibrahim K Onal; Mevlut Kurt; Kadri Altundag; Sercan Aksoy; Murat Dincer; Ibrahim Gullu
Journal:  Med Oncol       Date:  2006       Impact factor: 3.064

2.  Primary immunodeficiency diseases in Latin America: the second report of the LAGID registry.

Authors:  Lily E Leiva; Marta Zelazco; Matías Oleastro; Magda Carneiro-Sampaio; Antonio Condino-Neto; Beatriz Tavares Costa-Carvalho; Anete Sevciovic Grumach; Arnoldo Quezada; Pablo Patiño; José Luis Franco; Oscar Porras; Francisco Javier Rodríguez; Francisco Javier Espinosa-Rosales; Sara Elva Espinosa-Padilla; Diva Almillategui; Celia Martínez; Juan Rodríguez Tafur; Marilyn Valentín; Lorena Benarroch; Rosy Barroso; Ricardo U Sorensen
Journal:  J Clin Immunol       Date:  2006-12-27       Impact factor: 8.317

3.  Expansion of T helper type 17 lymphocytes in patients with chronic granulomatous disease.

Authors:  R Horváth; D Rožková; J Lašťovička; A Poloučková; P Sedláček; A Sedivá; R Spíšek
Journal:  Clin Exp Immunol       Date:  2011-10       Impact factor: 4.330

Review 4.  TH17 deficiency in human disease.

Authors:  Douglas R McDonald
Journal:  J Allergy Clin Immunol       Date:  2012-05-01       Impact factor: 10.793

5.  Multiple reversions of an IL2RG mutation restore T cell function in an X-linked severe combined immunodeficiency patient.

Authors:  Tomoki Kawai; Megumu Saito; Ryuta Nishikomori; Takahiro Yasumi; Kazushi Izawa; Tomohiko Murakami; Shigefumi Okamoto; Yasuko Mori; Noriko Nakagawa; Kohsuke Imai; Shigeaki Nonoyama; Taizo Wada; Akihiro Yachie; Katsuyuki Ohmori; Tatsutoshi Nakahata; Toshio Heike
Journal:  J Clin Immunol       Date:  2012-03-30       Impact factor: 8.317

6.  Clearance of Staphylococcus aureus nasal carriage is T cell dependent and mediated through interleukin-17A expression and neutrophil influx.

Authors:  Nathan K Archer; Janette M Harro; Mark E Shirtliff
Journal:  Infect Immun       Date:  2013-03-25       Impact factor: 3.441

7.  Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency.

Authors:  Tuba Turul; Ilhan Tezcan; Hasibe Artac; Sandra de Bruin-Versteeg; Barbara H Barendregt; Ismail Reisli; Ozden Sanal; Jacques J M van Dongen; Mirjam van der Burg
Journal:  Eur J Pediatr       Date:  2008-05-29       Impact factor: 3.183

8.  Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8.

Authors:  Manda L Waldrep; Yingxin Zhuang; Harry W Schroeder
Journal:  BMC Med Genet       Date:  2009-09-23       Impact factor: 2.103

Review 9.  Gene Therapy for X-Linked Severe Combined Immunodeficiency: Where Do We Stand?

Authors:  Marina Cavazzana; Emmanuelle Six; Chantal Lagresle-Peyrou; Isabelle André-Schmutz; Salima Hacein-Bey-Abina
Journal:  Hum Gene Ther       Date:  2016-02       Impact factor: 5.695

Review 10.  Gene therapy for severe combined immunodeficiency: are we there yet?

Authors:  Marina Cavazzana-Calvo; Alain Fischer
Journal:  J Clin Invest       Date:  2007-06       Impact factor: 14.808

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