Sympathetic Ophthalmia (SO)
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Sympathetic Ophthalmia (SO)

The development of therapies for sympathetic ophthalmia (SO) necessitates a multidisciplinary approach involving refined diagnostics, directed immunosuppression, and biologic therapeutic modalities. Protheragen appreciates that each customer has distinct needs. Because of this, our specialized services offer customizable plans that target particular needs associated with the diagnosis and therapeutic gaps for sympathetic ophthalmia.

Overview of Sympathetic Ophthalmia (SO)

Sympathetic ophthalmia (SO) is an uncommon bilateral condition involving granulomatous panuveitis that usually occurs after penetrating trauma to one eye or a surgical procedure. An autoimmune reaction takes place wherein the sympathizing eye without injury develops inflammatory changes due to the trauma or surgery applied on the exciting eye. The interval between initial trauma and symptom presentation is quite variable, anywhere from a few days to several years, although most cases present within 3 months, and 90% present within a year of the injury. SO is a critical condition which, without prompt therapeutics, can severely damage sight, or even lead to blindness.

Schematic representation of antigenic peptide presentation by antigen-presenting cells (APCs) to autoreactive CD4+ cells.Fig.1 After the inciting event, the antigen-presenting cells (APC) present the antigen peptide to autoreactive CD4+ cells. (Paulbuddhe V., et al., 2021)

Diagnostics Development for Sympathetic Ophthalmia (SO)

  • Fundus Fluorescein Angiography (FFA)
    It shows distinct angiographic patterns like pinpoint hyperfluorescent leakage and hypofluorescent spots with later-phase dye pooling.
  • Indocyanine Green Angiography (ICGA)
    ICGA demonstrates hypocyanescent areas due to infiltration of choroidal edema or infiltrates which may persist or fade depending on the stage of the condition.
  • Optical Coherence Tomography (OCT)
    OCT captures detailed and high-resolution images of the choroid and retina, enabling evaluators to monitor and assess structural changes.
  • Ultrasound B-Scan
    This imaging method provides a high degree of detail concerning choroidal thickening and serous retinal detachment, thus aiding in the diagnosis and follow-up of SO.

Therapeutics of Sympathetic Ophthalmia (SO)

Therapeutics Target Description Research Stage
Corticosteroids General Inflammation High-dose systemic corticosteroids are the first line of therapeutics. They rapidly reduce inflammation but are associated with significant side effects. Approved
Azathioprine Immune System An immunomodulatory agent that inhibits purine synthesis, reducing the activity of T and B lymphocytes. Used to spare corticosteroids and manage long-term therapeutics. Approved
Methotrexate Immune System A folic acid analogue that inhibits dihydrofolate reductase, reducing the proliferation of rapidly dividing cells. Effective in managing chronic inflammation. Approved
Mycophenolate Mofetil Immune System Inhibits inosine monophosphate dehydrogenase, reducing purine synthesis and lymphocyte proliferation. Used in refractory cases. Approved
Cyclosporine Immune System A calcineurin inhibitor that suppresses T-cell activation, reducing inflammation. Often used in combination with corticosteroids. Approved
Cyclophosphamide Immune System An alkylating agent used in severe, refractory cases. It has significant toxicity and is used as a last resort. Approved
Infliximab TNF-α A monoclonal antibody that binds to TNF-α, reducing inflammation. Used in refractory cases where traditional immunosuppressive agents fail. Approved
Adalimumab TNF-α A fully humanized monoclonal antibody against TNF-α, used in refractory cases and approved by the FDA for non-infectious uveitis. Approved
Tocilizumab IL-6 Receptor An IL-6 receptor antagonist used in refractory cases, showing promise in controlling inflammation. Approved
Intravitreal Steroids Local Inflammation Intravitreal injections or implants (e.g., dexamethasone, fluocinolone acetonide) to reduce intraocular inflammation and spare systemic corticosteroids. Approved

Disclaimer: Protheragen focuses on providing preclinical research service. This table is for information exchange purposes only. This table is not a treatment plan recommendation. For guidance on treatment options, please visit a regular hospital.

Our Services

Protheragen provides a full range of services for the diagnostics and therapeutics development of sympathetic ophthalmia. This includes an all-embracive service of scope from initial research through to advanced preclinical trials, guaranteeing that clients receive bespoke services tailored to their requirements.

Diagnostics Development

  • Karyotype Analysis Service
  • Omics Analysis Service
  • Biomarker Development Service
  • Artificial Intelligence Service

Therapeutic Development

  • Small Molecule Drug
  • Cell Therapy
  • Gene Therapy
  • Therapeutic Antibody
  • Therapeutic Peptide
  • Therapeutic Protein

Preclinical Research

  • Pharmacodynamics Study Services
  • Pharmacokinetics Study Services
  • Drug Safety Evaluation Services

Disease Models

  • S Antigen-Induced Uveoretinitis Models
  • Rhodopsin-Induced Uveoretinitis Models
  • Interphotoreceptor Retinoid-Binding Protein (IRBP)-Induced Uveoretinitis Models
  • Recoverin-Induced Uveoretinitis Models

Recognizing the unique challenges posed by sympathetic ophthalmia, Protheragen's team of specialists is dedicated to developing customized preclinical research solutions to address the specific needs of our clients. If you are interested in our services, please feel free to contact us.

References

  • Paulbuddhe, Vivek, et al. "Sympathetic Ophthalmia (SO): where do we currently stand on treatment strategies?." Clinical Ophthalmology (2021): 4201-4218.
  • Parchand, Swapnil, et al. "Sympathetic Ophthalmia (SO): A comprehensive update." Indian Journal of Ophthalmology 70.6 (2022): 1931-1944.