Safety and Efficacy of Topical Infliximab in Autoimmune Dry Eye Disease

Inclusion Criteria: * Adult patients (≥ 18 years). * Confirmed diagnosis of primary or secondary Sjögren's syndrome according to the 2016 ACR/EULAR classification criteria. * On stable systemic immunomodulatory therapy (non-biologic) for at least 12 weeks, with no planned changes during the study (see section 14.1 if there are concerns about confounding variables). * Negative chest X-ray or Interferon-Gamma Release Assays (IGRA). * Diagnosis of severe dry eye, defined by meeting all of the following criteria in at least one eye at study entry: * OSS (SICCA 0-12) ≥ 6 in at least one eye. * OSDI ≥ 33 (severe symptoms). * Symptoms: OSDI score ≥ 33. * Signs: Ocular Staining Score (OSS, SICCA) ≥ 6. * Ability to understand and sign informed consent and to comply with study procedures and treatment administration. Exclusion Criteria: * Current use of topical corticosteroids or topical immunomodulators (cyclosporine, lifitegrast, tacrolimus, autologous serum) within 30 days prior to enrollment. * Current or recent use (\< 3 months) of punctal plugs. * Active ocular infection (bacterial, viral, fungal) or recent history of herpetic keratitis. * Ocular or eyelid surgery within the past 6 months. * Use of contact lenses during the study period. * Known allergy or hypersensitivity to infliximab, murine proteins, or any component of the formulation (including CMC). * Coexisting ocular conditions that may interfere with dry eye evaluation (e.g., active ocular cicatricial pemphigoid, active ocular graft-versus-host disease, uncontrolled glaucoma, significant corneal dystrophy). * Systemic conditions considered contraindications to infliximab exposure, including: active systemic infection, untreated active or latent tuberculosis, history of demyelinating disease, moderate to severe congestive heart failure (NYHA Class III/IV), or history of malignancy within the past 5 years. * Use of systemic biologic agents within the past 6 months (12 months for systemic anti-TNF-α therapy). * Pregnancy, breastfeeding, or intention to become pregnant during the study. * Participation in another clinical trial with an investigational drug within the past 30 days. * Ability to understand and sign informed consent and to comply with study procedures and treatment administration.