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Abstract Number: 0534

Lymphatic Dysfunction in Murine Lupus Photosensitivity

William Ambler1, Noa Schwartz2, Jin Yeon Shin3, Rahgu Kataru4, Camila Carballo5, Scott Rodeo6, Babak Mehrara4 and Theresa Lu7, 1Division of Pediatric Rheumatology, Department of Rheumatology, Hospital for Special Surgery. HSS Research Institute, Hospital for Special Surgery, New York, NY, 2Department of Medicine, Division of Rheumatology, Albert Einstein College of Medicine, New York, NY, 3Department of Surgery, Division of Plastic and Reconstructive Surgery Memorial Sloan Kettering, New York, NY, 4Department of Surgery, Division of Plastic and Reconstructive Surgery, Memorial Sloan Kettering, New York, NY, 5HSS Research Institute, Hospital for Special Surgery, New York, NY, 6HSS Research Institute, Hospital for Special Surgery; Department of Orthopedics, Hospital for Special Surgery, New York, NY, 7Hospital for Special Surgery, New York, NY

Meeting: ACR Convergence 2021

Keywords: Animal Model, autoimmune diseases, immunology, Mouse Models, Lupus, Systemic lupus erythematosus (SLE)

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Session Information

Date: Sunday, November 7, 2021

Title: SLE – Animal Models Poster (0534–0540)

Session Type: Poster Session B

Session Time: 8:30AM-10:30AM

Background/Purpose: The lymphatic system is composed of vessels which carry fluid, soluble molecules, and cells from peripheral tissue to draining lymph nodes. Photosensitivity, an exaggerated inflammatory response in response to ultraviolet radiation (UVR), is present in most patients with Systemic Lupus Erythematosus (SLE). Lymphatic dysfunction has been shown to induce photosensitivity in wild-type models, thus we hypothesized that lymphatic dysfunction could contribute to photosensitivity in SLE.

Methods: We examined MRL/lpr lupus prone mice for lymphatic function by injecting Evan’s Blue into the ear and measuring retention. Ear thickness and flow cytometric analysis were used to assess photosensitivity. This was similarly done in an inducible lupus model using chronic epicutaneous application of imiquimod on B6 mice. We then investigated the utility of improving lymphatic drainage using two approaches. First, we used manual lymphatic drainage (MLD) in the MRL/lpr mice. Second, we used the imiquimod inducible lupus phenotype in a novel mouse model with enhanced lymphatic function (inducible lymphatic endothelial cell specific PTEN KO).

Results: MRL/lpr mice had greater Evan’s blue retention compared to controls suggesting lupus prone mice have impaired lymphatic drainage. MLD improved lymphatic drainage and reduced photosensitivity. Imiquimod treated PTEN KO mice had reduced photosensitivity and reduced systemic immune activation compared with imiquimod treated controls.

Conclusion: This data suggests that lymphatic dysfunction contributes to photosensitivity in murine lupus and improving lymphatic flow, even with simple MLD, can ameliorate photosensitivity. Future studies will determine the etiology of lymphatic dysfunction in murine lupus and the mechanism of lessened photosensitivity with improved lymphatic drainage. If similar immune circuitry defects are present in patients with SLE, altering lymphatics could be a novel target for new therapeutics.


Disclosures: W. Ambler, None; N. Schwartz, None; J. Shin, None; R. Kataru, None; C. Carballo, None; S. Rodeo, None; B. Mehrara, Puretech corp, 2, Regeneron, 12, Investigator initiated research award; T. Lu, None.

To cite this abstract in AMA style:

Ambler W, Schwartz N, Shin J, Kataru R, Carballo C, Rodeo S, Mehrara B, Lu T. Lymphatic Dysfunction in Murine Lupus Photosensitivity [abstract]. Arthritis Rheumatol. 2021; 73 (suppl 9). https://acrabstracts.org/abstract/lymphatic-dysfunction-in-murine-lupus-photosensitivity/. Accessed .
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