
Vitamin D, VDR and antimicrobial peptides: mechanisms and clinical limits
Local vitamin D metabolism, VDR, CAMP and DEFB4: enzymes, compartments, LL-37 maturation and the limits of clinical infection prevention.

Local vitamin D metabolism, VDR, CAMP and DEFB4: enzymes, compartments, LL-37 maturation and the limits of clinical infection prevention.

Why food-specific IgG4 neither diagnoses intolerance nor guarantees safety. IgE/FcεRI signalling, IgG4 exchange, BAT, coeliac disease and actual LEAP, EAT, PALISADE and OUtMATCH findings.

Zinc-dependent thymulin activity, transport and TCR signaling; age-related involution, positive and negative trials, laboratory limitations, and safety.

How green tea EGCG interacts with DNMT, FOXP3, NF-κB and mTOR, why mouse findings do not establish stable human Treg, and what clinical studies show about efficacy and liver safety.

EPA/DHA enzymatic pathways, stereochemistry, receptors and efferocytosis. Analytical limits of SPM measurements and findings from small studies, REDUCE-IT, STRENGTH and GAUDI.

STAT3, NF-κB and NAD⁺-dependent deacetylation; conflicting Th17/Treg findings, pharmacokinetics and positive and negative clinical trials.

How lactoferrin coordinates Fe³⁺, how lactoferricin and other experimental mechanisms are studied, and what trials show for preterm sepsis, anemia, H. pylori, and respiratory infections.

How GML amphiphilicity changes membranes, why activity depends on the medium, and what short human topical studies actually found. Covers viral spectrum, cell signaling, hydrolysis, and the absence of an established oral treatment regimen.

Structure of β-(1→3)/(1→6)-glucans, Dectin-1 recognition, and cellular trained-immunity models; human studies of yeast and mushroom products, safety, and limits on extrapolating results.

What is known about elderberry cyanidin anthocyanins and neuraminidase, the limits of pharmacokinetic evidence, and why small positive trials coexist with a negative RCT in PCR-confirmed influenza. Raw-material safety and the absence of a universal dose are considered separately.

Echinacea alkylamide chemistry, CB2-dependent and independent cellular responses, human pharmacokinetics, and mixed clinical findings, with limits on extrapolation.

Andrographis paniculata chemistry, the preclinical Cys62 p50 NF-κB mechanism, trials of specific extracts for ARI symptoms, pharmacokinetics, and current allergy-safety signals.

How mast-cell receptors and calcium signals work, what quercetin and luteolin studies show, and why cell mechanisms do not establish direct CRAC blockade or MCAS treatment.

How to distinguish MCAS from mastocytosis and allergy; event-related tryptase, histamine, PGD₂, leukotrienes, diagnostic criteria, treatment evidence, and safety limits.

A professional review of bacterial wall composition, MDP access to NOD2, signaling and genetic pathways, and the limits of clinical evidence for specific inactivated preparations.

How the S100A8/S100A9 complex reaches stool from neutrophils, what the assay measures, and why thresholds differ for suspected IBD, remission monitoring, and postoperative follow-up.

How secretory IgA is assembled and transported across the epithelium, how it can limit pathogens while supporting some commensals, and why stool sIgA alone is not a diagnosis or treatment target.

How tributyrin and sodium butyrate differ in chemistry, lipolysis, release location, and clinical evidence—and why molecular composition alone does not prove delivery to the colon.

How berberine affects AMPK, MLCK, ZO-1, and occludin in epithelial injury models; pharmacokinetics, separate IBS-D and ulcerative-colitis findings, and limits of clinical inference.