Jean KANITAKIS

Prof. Dr. Jean KANITAKIS

Department of Dermatology, Ed. Herriot Hospital, 69003 Lyon, France
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Research Focus & Metrics

Academic Career Length

31Years (1996-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2020 in Journal of the American Academy of Dermatology
Verified
Journal Article
Closed access
Jean KANITAKISJean KANITAKIS
Jean KANITAKIS
CLCécile Lesort
Cécile Lesort
MDMarie Danset
Marie Danset
DJDenis Jullien
Denis Jullien

12 August 2010 in Experimental Dermatology
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Journal Article
Open access
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Jean KANITAKISJean KANITAKIS
Jean KANITAKIS
EMEmmanuel Morelon
Emmanuel Morelon
PPPalmina Petruzzo
Palmina Petruzzo
LBLionel Badet
Lionel Badet
JDJean‐Michel Dubernard
Jean‐Michel Dubernard
Abstract:  Epidermal Langerhans cells (LC) are dendritic, antigen‐presenting cells residing within mammalian epidermis and mucosal epithelia. When massively depleted, they are replaced by cells of bone‐marrow origin. However, their renewal within normal skin under steady‐state conditions is not precisely known. We observed that epidermal LC within a human hand allograft remain stable in the long term (10 years) and are not replaced by cells of recipient’s origin; furthermore, we observed a Langerhans cell in mitosis within the epidermis 8 years postgraft. These results show that under almost physiological conditions, human LC renew in the epidermis by local mitoses of preexisting cells.

20 August 2014 in Transplant International
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Journal Article
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Jean KANITAKISJean KANITAKIS
Jean KANITAKIS
GKGeorgia Karayannopoulou
Georgia Karayannopoulou
MLMarco Lanzetta
Marco Lanzetta
PPPalmina Petruzzo
Palmina Petruzzo
Whereas vascularized composite allografts often undergo acute rejections early in the postgraft period, rejection manifesting with severe vascular changes (graft vasculopathy) has only been observed on three occasions in humans. We report a hand-allografted patient who developed severe rejection following discontinuation of the immunosuppressive treatment. It manifested clinically with erythematous maculopapules on the skin and pathologically with graft vasculopathy that affected both large vessels and smaller cutaneous ones. The observation that graft vasculopathy can affect skin vessels shows that it is amenable to diagnosis with usual skin biopsy as recommended for the follow-up of these allografts. Graft vasculopathy developing in the setting of vascularized composite allografts likely represents chronic rejection due to under-immunosuppression and, if confirmed, should be included in a future update of the Banff classification of vascularized composite allograft rejection.

1 September 2015 in Journal of Plastic, Reconstructive & Aesthetic Surgery
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Journal Article
Closed access
LBLaurence Bernardon
Laurence Bernardon
AGAram Gazarian
Aram Gazarian
PPPalmina Petruzzo
Palmina Petruzzo
TPTara Packham
Tara Packham
MGMichel Guillot
Michel Guillot
LBLionel Badet
Lionel Badet

1 July 2011 in Dermatology Online Journal
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Journal Article
Closed access
KKKyriakos Kyamidis
Kyriakos Kyamidis
VLViviana Lora
Viviana Lora
Jean KANITAKISJean KANITAKIS
Jean KANITAKIS
Author(s): Kyamidis, Kyriakos; Lora, Viviana; Kanitakis, Jean

28 January 2024 in American Journal of Transplantation
Verified
Journal Article
Open access
LCLinda C. Cendales
Linda C. Cendales
AFAlton B. Farris
Alton B. Farris
IRIvy Rosales
Ivy Rosales
DEDavid Elder
David Elder
AGArmando Gamboa-Domínguez
Armando Gamboa-Domínguez
MSMaria Angelica Selim
Maria Angelica Selim
As more data becomes available, the Banff 2007 working classification of skin-containing vascularized composite allograft (VCA) pathology is expected to evolve and develop. This report represents the Banff VCA Working Group's consensus on the first revision of the 2007 scoring system. Prior to the 2022 Banff-CST Joint Meeting, eighty-three clinicians and/or researchers were invited to a virtual meeting to discuss whether the 2007 Banff VCA system called for a revision. Unanimously, it was determined that the vascular changes were to be included in the first revision. Subsequently, two international online surveys, each followed by virtual discussions, were launched. The goals were: 1) to identify which changes define severe rejection, 2) to grade their importance in the evaluation of severe rejection, 3) to identify emerging criteria to diagnose rejection. A final hybrid (in person and virtual) discussion at the Banff/CST join meeting finalized the terminology, the definition, a scoring system, and a reporting system of the vascular changes. This proposal represents an international consensus on this topic and establishes the first revision of the Banff 2007 working classification of skin-containing vascularized composite allograft pathology.