J.H. Saurat
University of Michigan
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Featured researches published by J.H. Saurat.
British Journal of Dermatology | 2003
Charles N. Ellis; Thomas A. Luger; D. Abeck; R. Allen; R.A.C. Graham‐Brown; Y. De Prost; L.F. Eichenfield; C. Ferrandiz; Alberto Giannetti; J. Hanifin; J.Y.M. Koo; D. Leung; C. Lynde; J. Ring; R. Ruiz‐Maldonado; J.H. Saurat
C . E L L I S * A N D T . L U G E R † O N B E H A L F O F T H E I C C A D I I F A C U L T Y : D . A B E C K , R . A L L E N , R . A . C . G R A H A M B R O W N , Y . D E P R O S T , L . F . E I C H E N F I E L D , C . F E R R A N D I Z , A . G I A N N E T T I , J . H A N I F I N , J . Y . M . K O O , D . L E U N G , C . L Y N D E , J . R I N G , R . R U I Z M A L D O N A D O A N D J H . S A U R A T
British Journal of Dermatology | 1975
J.H. Saurat; Eliane Gluckman; Anette Bussel; Liliane Didierjean; A. Puissant
A lichen planus‐like eruption was seen in four patients after bone marrow transplantation. The skin and mucous membrane appearance closely mimicked lichen planus. The histopathology was also very similar to lichen planus. The occurrence of a lichen planus‐like eruption (LPLE) after an immune basal cell damage related to the graft‐versus‐host reaction raised the question of the immune nature of this eruption. The correlation found between biological signs of graft‐versus‐host reaction and the outbreak or relapse of the lichen planus‐like eruption supports the hypothesis that the skin changes could be a sign of a chronic immune response against recipient epidermis.
British Journal of Dermatology | 2010
Diamant Thaçi; J.P. Ortonne; Sergio Chimenti; Pierre-Dominique Ghislain; P. Arenberger; K Kragballe; J.H. Saurat; A Khemis; P Sprøgel; H-U Esslinger; Kristina Unnebrink; H Kupper
Background Data are lacking on the use of topical therapies in combination with tumour necrosis factor blockers for the treatment of psoriasis.
Journal of The European Academy of Dermatology and Venereology | 2005
Johannes Ring; Jnwn Barker; H. Behrendt; L. Braathen; Ulf Darsow; Louis Dubertret; Alberto Giannetti; J.L.M. Hawk; H. Honigsmann; Lajos Kemény; Thomas A. Luger; M. Meurer; G.M. Murphy; Annamari Ranki; T. Reunala; J.H. Saurat; W. Sterry; P.C.M. van de Kerkhof
ABSTRACT Topical Calcineurin Inhibitors (TCIs) used for the treatment of atopic eczema modify the immune regulatory function of the skin and may have the potential to enhance immunosuppressive ultraviolet (UV) effects. Current recommendations on UV protection in eczema patients treated with PCIs are inconsistent and have given rise to uncertainty and anxiety in patients. Therefore, the European Dermatology Forum (EDF) developed a position statement which reviews critically the available data with regard to the problem, especially analysing and commenting the limitations of rodent models for the human situation. There is no conclusive evidence from rodent trials to indicate that long‐term application of TCIs is photococarcinogenic. There is a need for further studies to investigate the validity of mouse models as well as long‐term cohort studies in patients using TCIs. Available data suggest that long‐term application of TCIs is safe, that there is no evidence of increased skin cancer risk and that it is ethical to treat patients with TCIs when indicated.
Clinical and Experimental Dermatology | 1976
J.H. Saurat; Jean-Marie Bonnetblanc; Eliane Gluckman; Liliane Didierjean; Annette Bussel; A. Puissant
Direct and indirect immunofluorescent studies were performed in seventeen bone marrow transplanted patients (BMT). No immunoglobulins were found in the maculo papular lesions of the early graft versus host reaction. Globular deposits of IgM and complement were found in the skin specimens from lichen planus like eruptions; these were very similar to those found in idiopathic lichen planus. Circulating epidermal cytoplasmic antibodies (ECA) were detected in 15 of 17 (88%) patients as shown by a longitudinal study of 118 sera. This frequency was significantly higher than in other groups in this study (133 subjects). ECA did not correlate with a graft versus host reaction. It is postulated that they develop as a consequence of chronic skin damage in subjects with disorders of the immune system which stimulate the production of numerous antibodies.
British Journal of Dermatology | 1992
H. S. I. Anttila; Sakari Reitamo; J.H. Saurat
Interleukin 1 (IL‐1) immunoreactivity in sebaceous glands was studied in paraffin sections of normal human skin. A panel of antibodies against IL‐1α and β was tested using an immunoperoxidase labelling method. All the antibodies showed a similar specific labelling pattern: both glandular and ductal cells were immunoreactive for both IL‐1α and β, provided optimal tissue fixation was used.
British Journal of Dermatology | 1990
Sakari Reitamo; H. S. I. Anttila; Liliane Didierjean; J.H. Saurat
Bouin‐fixed paraffin sections or acetone‐fixed cryostat sections were labelled with the avidinbiotin complex (ABC) or peroxidase‐antiperoxidase (PAP) method using three monoclonal antibodies (MAbs) and two polyclonal antisera to human recombinant interleukin i beta (IL‐iβ) and three polyclonal antisera to human recombinant interleukin iα (IL‐iα). In the secretory coil both IL‐α and β were detected in the clear, but not in the dark cells. Both luminal and basal cells of the coiled and straight ducts expressed IL‐iα and β, the IL‐i labelling being more intense in the luminal cells. IL‐i was not usually detected in the initial portion of the intraepidermal eccrine sweat duct, whereas intense labelling was seen in the upper part including through the stratum corneum. In skin biopsies of the palm, taken after exercise, there was only faint IL‐i labelling of the secretory cells, whereas the luminal cells of the dermal ducts showed intense labelling for both IL‐iα and β. In the acrosyringium, exercise did not alter the pattern for IL‐iα and β, except that in the palm, some of the antibodies to IL‐iβ produced a more intense immunolabelling of the acrosyringeal cells. This study identifies a distinct and similar distribution of the two forms of IL‐i throughout the eccrine sweat‐gland apparatus and indicates that part of the IL‐i epidermal pool originates from the sweat.
British Journal of Dermatology | 1978
J.H. Saurat; Liliane Didierjean; F. Beucher; Eliane Gluckman
Sera with epidermal cytoplasmic antibodies (E.C.A.) produced by human subjects after bone marrow transplantation have been studied by indirect immunofluorescence on rabbit lip sections. These sections were used in order to give on a single specimen, areas of mucosa, of parakeratotic and of orthokeratotic epithelium. It has been demonstrated that E.C.A. distinguished the basal cell layer from the upper cell layers on the three areas. Moreover, E.C.A. were not found to react identically on mucosal, parakeratotic and orthokeratotic epithelium. These findings strongly suggest that the target antigens for E.C.A. are molecules involved in keratinocyte differentiation.
British Journal of Dermatology | 2003
Gewirtzman Aj; J.H. Saurat; Braun Rp
Summary Background Dermoscopy, a noninvasive technique used to help physicians better visualize pigmented skin lesions, is becoming widely used by dermatologists. Yet despite its popularity, to our knowledge basic aspects such as the best immersion fluid (IF) to use and proper procedures for applying the IF and dermatoscope have never been the subject of a systematic investigation.
Clinical and Experimental Dermatology | 1980
Liliane Didierjean; J.H. Saurat
Using human sera obtained from bone marrow transplant recipients which contain antibodies to cytoplasmic epidermal antigens, we have found a cross reactivity between epidermis and thymus in immunofluorescence. The shared antigen(s) were only localized in the Hassalls corpuscle on the thymus and the upper (stratum spinosum) compartment of the epidermis. The basal cell layer did not show shared antigens. Antigenic similarity between epidermis and thymus may thus be restricted to a subset of keratinocytes.