Biology subjects

Mihai, A.

Publications and source records attributed to Mihai, A..

3 recordsLinked to original sources

bioRxiv2026

Species responses to nutrient loading promote resistance but not temporal stability in floating macrophyte communities

Determining the drivers of ecological stability amid accelerating global environmental change is a critical goal of contemporary ecology. Various candidate drivers have been suggested, with recent attention turning to response diversity--the variation among organism-environment responses. However, despite conceptual interest in response diversity as a driver of stability, there remain few field tests of this relationship. Using multi-species competitive communities of floating aquatic macrophytes as an experimental model for measuring temporal stability and response diversity to nutrient loading, we show that response diversity does not promote temporal stability of total macrophyte cover, but that communities with an uneven distribution of species responses were more resistant to an exogenous shock. To quantify macrophyte composition and growth dynamics from photographic time series of our experimental communities, we developed an open-source, scalable, machine learning workflow (LeafMosaic) capable of classifying four species from noisy field data including variable lighting, resolution, and plant morphology. We measured response diversity as the balance of positive and negative biomass growth responses to dissolved nitrate concentration, weighted by species relative contributions to biomass, and tested its effect on temporal stability and resistance to an unexpected pulse disturbance (a large typhoon that disrupted our outdoor mesocosms). Response imbalance predicted typhoon resistance, but species asynchrony and mean population stability best predicted community stability, with no direct or indirect effect of species responses. Overall, our results provide new experimental evidence for how the structure of species responses promotes stability, and we aim our LeafMosaic workflow to empower future field experiments using floating macrophytes to study response diversity and ecological stability.

ecology↗

bioRxiv2025

Neoadjuvant anti-4-1BB confers protection against spontaneous metastasis through low-affinity intratumor CD8+ T cells in triple-negative breast cancer

Neoadjuvant immunotherapy seeks to harness the primary tumor as a source of relevant tumor antigens to enhance systemic anti-tumor immunity through improved immunological surveillance. Despite having revolutionized the treatment of patients with high-risk early-stage triple-negative breast cancer (TNBC), a significant portion of patients remain unresponsive and succumb to metastatic recurrence post-treatment. Here, we found that optimally scheduled neoadjuvant administration of anti-4-1BB monotherapy was able to counteract metastases and prolong survival following surgical resection. Phenotypic and transcriptional profiling revealed enhanced 4-1BB expression on tumor-infiltrating intermediate (Tint), relative to progenitor (Tprog) and terminally exhausted (Tterm) T cells. Furthermore, Tint was enriched in low-affinity T cells. Treatment with anti-4-1BB drove clonal expansion of Tint, with reduced expression of tissue-retention marker CD103 in Tprog. This was accompanied by increased TCR clonotype sharing between paired tumors and pre-metastatic lungs. Further interrogation of sorted intratumor T cells confirmed enhanced T cell egress into circulation following anti-4-1BB treatment. In addition, gene signature extracted from anti-4-1BB treated Tint was consistently associated with improved clinical outcomes in BRCA patients. Combinatorial neoadjuvant anti-4-1BB and ablation of tumor-derived CXCL16 resulted in enhanced therapeutic effect. These findings illustrate the intratumor changes underpinning the efficacy of neoadjuvant anti-4-1BB, highlighting the reciprocity between local tissue-retention and distant immunologic fortification, suggesting treatment can reverse the siphoning of intratumor T cells to primary tumor, enabling redistribution to distant tissues and subsequent protection against metastases.

immunology↗

bioRxiv2024

E protein control of NKgammadeltaT cell development through both generation and function of the stereotypic Vgamma1Vdelta6.3 TCR

T cell receptor (TCR) signals regulate important developmental transitions through induction of the E protein antagonist, Id3; however, Id3-deficiency produces paradoxical effects on {gamma}{delta} T cell subsets. Here, we show here that Id3-deficiency attenuates the development of V{gamma}3-expressing {gamma}{delta} T cells, while markedly enhancing the development of V{gamma}1V{delta}6.3-expressing NK{gamma}{delta}T cells. Id3-deficiency does so by regulating both the generation of the stereotypic V{gamma}1V{delta}6.3 TCR expressed by NK{gamma}{delta}T cells and its capacity to support development. Indeed, we determined that the Trav15 segment, which encodes the V{delta}6.3 TCR subunit, is directly bound by E proteins that control its expression. Moreover, once expressed, the resulting V{gamma}1V{delta}6.3 TCR in capable of specifying the innate-like NK{gamma}{delta}T cell fate in a cell-autonomous and developmentally-unrestricted manner that is restrained by the Id3/E axis. Together, these data indicate that the paradoxical behavior of NK{gamma}{delta}T cells in the Id3-deficient setting is entirely determined by its stereotypic V{gamma}1V{delta}6.3 TCR complex.

immunology↗