We thank our colleagues Venkatesh et al for their interest and detailed observations regarding our multicenter collaborative study for generating consensus amongst physicians for initiating antitubercular therapy (ATT) in patients with tubercular (TB) choroiditis. 1 The Collaborative Ocular Tuberculosis Study (COTS) consensus underlines that if a treating uveitis expert does not believe that the diagnosis is consistent with tubercular uveitis (TBU), there is no mandate that the expert must treat with ATT. 1,2 Our esteemed colleagues state that the participants in the study have a strong bias toward the diagnosis of TB choroiditis and argued that the clinical photographs may have several differential diagnoses aside from TBU. We would like to highlight the statement in our results where we mention that the clinical scenarios discussed assumes the exclusion of other possible forms of uveitis masquerading as TBU and that the clinical photographs in Figure 2 are intended to illustrate the clinical phenotypes of TBU discussed for the benefit of the reader. 1,2 We would also like to refer Venkatesh et al to publications on choroidal involvement in TBU which have described acute posterior multifocal placoid pigment epitheliopathy as a rare phenotype associated with TB choroiditis. 3 With regard to the concerns of Venkatesh et al regarding the past treatment history and other clinical history, the survey participants were asked to assume that the scenarios considered did not involve patients with "active" systemic TB, or past history of ATT intake. 1,2 Although our colleagues state that "first attack" of choroiditis, bilaterality, and visual acuity should be considered before the initiation of ATT, this seems to be their personal opinion, because this is not universally agreed upon. 1,2 The authors also raised concerns regarding the use of the interferon-gamma release assay (IGRA) in diagnosing TBU. Venkatesh et al may be aware that IGRA has been discouraged by the World Health Organization for "active" pulmonary TB (not TBU) because it is unable to distinguish it from latent TB. For countries such as India that have banned IGRA, the survey specifically allowed an option "test not done/not available" (Appendix 2 in the original article). 1,2 We would also like to emphasize that in several countries, the tuberculin skin test is not permitted/available. The survey has considered these factors and was therefore designed to reflect a global scenario when evaluating the various permutations of investigations available in the clinical scenarios discussed. Separately, Venkatesh et al have also advocated the relevance of immunologic tests in diagnosing TBU using IGRA (both QuantiFERON Gold and T-SPOT.TB test