bioRxiv Science⌕ Search

bioRxiv · 10.64898/2026.10.12.758659

Innate Immune Correlates of Sickness-Like Depressive Symptoms in Breast Cancer Survivors

Abstract

Background: Research supports immune pathways of depression characterized by sickness-like symptoms (e.g., appetite changes, low energy, sleep disturbance, difficulty initiating activity, concentration difficulties), with limited evidence for negative affect symptoms (e.g., depressed mood, feeling of failure). However, most findings come from otherwise healthy individuals, limiting generalizability to medical populations. This study leveraged breast cancer as a disease context, given the lasting cancer- and treatment-related effects on immune function, to examine the hypothesis that proinflammatory gene expression relates more strongly to sickness-like than negative affect symptoms. Methods: Data were drawn from 175 women with Stage 0-III breast cancer (Mage=55.3 years) assessed at five time points from diagnosis through 18 months post-treatment. Depressive symptom dimensions were assessed using the Center for Epidemiologic Studies Depression Scale. Peripheral blood mononuclear cell gene expression was assessed using RNA sequencing-based transcriptional profiling. Primary analyses focused on proinflammatory gene expression. Exploratory analyses examined Type-I interferon gene expression and transcript-derived cell-type composition (myeloid-to-lymphoid and classical-to-non-classical monocyte ratios). Results: Longitudinal mixed-effects models across repeated assessment revealed that greater sickness-like symptom severity was associated with elevated proinflammatory gene expression (p<.001), Type-I Interferon antiviral gene expression (p<.001), myeloid cell abundance (p<.001), and particularly non-classical monocytes (p=.002). By contrast, negative affect symptoms showed weaker, null, or opposite associations. Conclusions: Sickness-like and negative affect symptoms show divergent associations with innate immune system activation and myeloid lineage bias. Results may inform more targeted interventions for both physical/energetic and psychological symptoms in breast cancer survivors, and may be relevant to other depression and medical contexts.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Chat, I. K.-Y., Cole, S. W., Bower, J. E.. 2026-10-19. Innate Immune Correlates of Sickness-Like Depressive Symptoms in Breast Cancer Survivors. https://doi.org/10.64898/2026.10.12.758659

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Stealth CAR-Tregs evade CD3 antibody therapy and skew immune responses toward regulation

Organ transplantation standard of care relies on lifelong immunosuppression, increasing infection and malignancy risks. An emerging approach using Chimeric Antigen Receptor Regulatory T cells (CAR-Tregs) targeting donor antigens, allows the suppression of alloimmune responses while preserving protective immunity. However, transplant recipients harbor a substantial pool of alloreactive memory T-cells, limiting CAR-Tregs tolerance-promoting effect. To address this challenge, our strategy combines selective depletion of activated T-cells, using non-mitogenic CD3 antibody therapy, with HLA-A2-targeted-CAR-Treg therapy. We established that T-cell receptor alpha chain (TRAC) deletion does not impair CAR-Treg antigen-specific activation, expansion, or their transcriptomic, phenotypic, epigenetic, and functional profiles. TRAC-/-CAR-Tregs exhibit robust protection from CD3 antibody depletion in circulation and peripheral tissues, whereas most TRAC+/+CAR-T cells are eliminated. Importantly, TRAC+/+CAR-T cells that escape CD3 antibody mediated depletion exhibit a transcriptomic signature consistent with T-cell exhaustion. Our findings demonstrate that CD3 antibody therapy provides an in vivo survival advantage to TRAC-/-CAR-Tregs, thereby shifting the immune balance toward regulation. This approach might enhance the translational potential of CAR-Treg therapy by reducing the required cell dose needed for clinical efficacy.

immunology↗

High-Throughput Screening Identifies Proteasome Inhibitors as Potentiators of Type III Interferon JAK-STAT Signaling and Antiviral Immunity

Type III interferon (IFN3, IFN{lambda}) drives antiviral defense at epithelial barriers with a more favorable safety profile than Type I interferon (IFN1), but weaker signaling limits its therapeutic potential. To identify small molecules that potentiate IFN-JAK-STAT signaling, we developed a high-throughput live-cell assay measuring STAT1/STAT2 phosphorylation in A549 cells and screened ~8,640 compounds. This identified proteasome inhibitors (MG132, delanzomib, ixazomib, oprozomib, bortezomib) as selective potentiators of IFN3-induced STAT activation, with minimal effect on IFN1 signaling. Proteasome inhibition enhanced IFN3 antiviral activity to levels approaching IFN1. Mechanistically, proteasome inhibition increased cell-surface IL10R{beta}, the limiting IFN3 receptor subunit, thereby increasing receptor JAK-STAT signaling. It did not alter IFN1 receptor levels but protected IFNAR2 from late ligand-induced downregulation. These findings establish receptor subunit availability as a rate-limiting, druggable node governing IFN3 signaling strength and demonstrate a scalable platform for identifying cytokine-selective signaling potentiators, with implications for mucosal antiviral therapeutics.

immunology↗

Identifying the immunocompetence markers at weaning to predict long-term vaccine response and persistence in pigs

Vaccination is a key strategy for controlling infectious disease in pigs, but the magnitude and persistence of vaccine-induced immunity vary among individuals. We investigated whether immune and physiological traits measured at weaning could predict long-term antibody (Ab) status and Ab persistence following vaccination against Mycoplasma hyopneumoniae (MH) and Influenza A virus (IAV), and whether predictive markers were shared between vaccines. Two vaccination trials were conducted in a cohort of 381 Large White pigs (MH, n=189; IAV, n=192). Animals were vaccinated at weaning (28 days of age) and received a booster 21 days later. Long-term Ab status was defined at 118 days post-vaccination (dpv) using assay-specific thresholds, while Ab persistence was defined as the decline from the individual peak response at 28 or 35 dpv to 118 dpv. A broad panel of immune and physiological traits measured at weaning was evaluated as candidate predictors. Sparse Partial Least Squares Discriminant Analysis (sPLS-DA) was used for variable selection, followed by PLS-DA classification models. Cross-validated accuracies ranged from 64.7% to 67.7%, indicating moderate predictive performance. Across vaccines, eight predictors were shared for long-term Ab status and twelve for Ab persistence. Hematocrit, IgG, platelet count, and plateletcrit (PCT) were associated with positive long-term Ab status for both vaccines, whereas mean corpuscular hemoglobin concentration (MCHC) and neutrophil percentage were associated with negative status. For persistence, higher vitamin D, -1 globulin concentration, platelet count, and PCT were consistently associated with persistent responses across vaccines, while MCHC and spectral absorbance traits were associated with non-persistence. These findings indicate that early-life immune and physiological traits measured at weaning are associated with immunocompetence traits that contribute to variation in subsequent long-term vaccine antibody outcomes and responsiveness. The identification of both shared and vaccine- or phenotype-specific predictors suggests that vaccine responsiveness reflects both general features of baseline immunocompetence and context-specific determinants.

immunology↗