Search bioRxiv⌕ Search

Biology subjects

Gorantla, A.

Publications and source records attributed to Gorantla, A..

2 recordsLinked to original sources

A Precisely Controlled Long-Acting Immunosuppression Platform Enables Prolonged Survival of Vascularized Composite Allografts

Vascularized composite allotransplantation (VCA) restores complex tissue defects but demands lifelong systemic immunosuppression. Oral tacrolimus (TAC) is limited by a narrow therapeutic window, pharmacokinetic variability, adherence challenges, and toxicity. Local delivery could mitigate these issues, yet clinical translation has been hindered by burst release, short duration, and the inability to co-deliver agents. We developed PRECISE (Programmable, REtrievable, Controlled ImmunoSuppression Encapsulator), an injectable, in-situ-forming PLGA depot that achieves long-acting, tightly controlled TAC release via structure-guided co-formulation with drug-binding agents (DBAs). GRAS small molecules (e.g., EGCG, maltotriose) identified by in silico docking and in vitro screening suppressed burst and modulated solvent efflux. Notably, rapamycin (RAPA) served dually as an mTOR inhibitor and a TAC-binding excipient, enabling synchronized dual-agent delivery. PRECISE eliminated burst in vitro and produced coordinated TAC+RAPA release with clinically compatible injectability. In rats, monthly intragraft dosing maintained systemic TAC/RAPA within the therapeutic window ([~]5-10 ng/mL) for >300 days, prolonged hindlimb allograft survival, expanded Tregs, and induced donor-specific hyporesponsiveness. Surgical retrieval of the depot triggered rapid TAC decline, demonstrating reversibility. In a stringent, fully MHC-mismatched porcine VCA model, PRECISE maintained on-target drug levels and extended graft survival beyond 90 days with minimal rejection and preserved vascular integrity. PRECISE is, to our knowledge, the first retrievable, injectable platform to deliver long-acting, dual-agent immunosuppression with controlled kinetics, rapid attainment of therapeutic steady state, and sustained graft protection. Its modular, structure-guided design enables clinical translation across VCA and solid-organ transplantation, delivering precise, durable, and safer immunosuppression.

bioengineering↗

TRB3 augments IL1β-TLR4 signaling by engaging Flightless-homolog 1.

Signaling via IL1{beta} and TLR4 receptors (IL1R-TLR4) plays a crucial role in cytokine and fatty acid-induced beta cell inflammation, in type 1 and type 2 diabetes respectively. IL1R-TLR4 share signaling mechanisms via a common, cytoplasmic, toll-like-receptor domain to activate proinflammatory JNK and IKK kinases. We have previously reported that in response to IL1{beta}, pancreatic islets isolated from TRB3 knockout (TRB3KO) mice show attenuated kinetics of activation for MAP3K MLK3, and JNK stress kinases. Here we report that similar to MLK3 and JNK, TRB3KO islets also show a decrease in amplitude and duration of IL1{beta}/LPS-stimulated TAK1 and IKK phosphorylation. Thus, loss of TRB3 attenuates both pathways critically required for a full-blown, cytokine-inducible, proapoptotic response in beta cells. TRB3KO islets display a sharp decrease in cytokine-induced beta cell death, accompanied by a decrease in select downstream NFkB targets, most notably, inducible Nitric Oxide Synthase (iNOS/NOS2), a well-characterized mediator of beta cell dysfunction and death. In order to better understand the molecular basis of TRB3-enhanced IL1R-TLR4 signaling, we interrogated the TRB3 interactome and identified Flightless-homolog 1 (Fli1), an immunomodulatory, actin-binding, leucine-rich-repeat protein, as a novel TRB3-interaction factor. TRB3 binds and disrupts Fli1-dependent sequestration of MyD88, thereby increasing availability of this proximal adaptor to participate in IL1R-TLR4 signaling. Fli1 forms a multiprotein complex that can disconnect IL1R-TLR4 from MyD88, resulting in a brake on assembly of downstream signaling complexes. By interacting with Fli1, TRB3 lifts the brake on IL1R-TLR4 signaling to augment the proinflammatory response in beta cells.

biochemistry↗