Efficacy of Allogeneic and Xenogeneic Exosomes for the Treatment of Canine Atopic Dermatitis: A Pilot Study
Sang-Won Kim,
Kyung-Min Lim,
Ssang-Goo Cho,
Bokyeong Ryu,
C-Yoon Kim,
Seon Young Park,
Kyungmin Jang,
Jae Heon Jung,
Cheolhyoung Park,
Chulhee Choi,
Jung-Hyun Kim
Affiliations
Sang-Won Kim
Department of Veterinary Internal Medicine, College of Veterinary Medicine, Konkuk University, Seoul 05029, Republic of Korea
Kyung-Min Lim
Department of Stem Cell and Regenerative Biotechnology, Molecular & Cellular Reprogramming Center and Institute of Advanced Regenerative Science, Konkuk University, Seoul 05029, Republic of Korea
Ssang-Goo Cho
Department of Stem Cell and Regenerative Biotechnology, Molecular & Cellular Reprogramming Center and Institute of Advanced Regenerative Science, Konkuk University, Seoul 05029, Republic of Korea
Bokyeong Ryu
Department of Veterinary Physiology, College of Veterinary Medicine, Konkuk University, Seoul 05029, Republic of Korea
C-Yoon Kim
Department of Veterinary Physiology, College of Veterinary Medicine, Konkuk University, Seoul 05029, Republic of Korea
Seon Young Park
ILIAS Biologics Inc., Daejeon 34014, Republic of Korea
Kyungmin Jang
ILIAS Biologics Inc., Daejeon 34014, Republic of Korea
Jae Heon Jung
ILIAS Biologics Inc., Daejeon 34014, Republic of Korea
Cheolhyoung Park
ILIAS Biologics Inc., Daejeon 34014, Republic of Korea
Chulhee Choi
ILIAS Biologics Inc., Daejeon 34014, Republic of Korea
Jung-Hyun Kim
Department of Veterinary Internal Medicine, College of Veterinary Medicine, Konkuk University, Seoul 05029, Republic of Korea
Canine atopic dermatitis (CAD) is a genetically predisposed inflammatory pruritic skin disease. The available treatments for CAD have several adverse effects and vary in efficacy, indicating the need for the development of improved treatments. In this study, we aimed to elucidate the therapeutic effects of allogeneic and xenogeneic exosomes on CAD. Six laboratory beagle dogs with CAD were randomly assigned to three treatment groups: control, canine exosome (cExos), or human exosome (hExos) groups. Dogs in the cExos and hExos groups were intravenously administered 1.5 mL of cExos (5 × 1010) and hExos (7.5 × 1011) solutions, respectively, while those in the control group were administered 1.5 mL of normal saline three times per week for 4 weeks. Skin lesion score and transepidermal water loss decreased in cExos and hExos groups compared with those in the control group. The exosome treatments decreased the serum levels of inflammatory cytokines (interferon-γ, interleukin-2, interleukin-4, interleukin-12, interleukin-13, and interleukin-31) but increased those of anti-inflammatory cytokines (interleukin-10 and transforming growth factor-β), indicating the immunomodulatory effect of exosomes. Skin microbiome analysis revealed that the exosome treatments alleviated skin bacterial dysbiosis. These results suggest that allogeneic and xenogeneic exosome therapy may alleviate CAD in dogs.