Temperature-dependent innate defense against the common cold virus limits viral replication at warm temperature in mouse airway cells
Cited in 2 Likelier entries (2 risks, 0 decisions).
Used in 2 entries
For each citing entry, the verbatim excerpt and Likelier's calculation notes (how the source's number was converted to the lifetime-probability framing) are shown below. Click through to read the full claim ledger.
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Rhinovirus replicates more robustly at 33–35 °C (nasal cavity) than at 37 °C (core body), with weaker interferon/antiviral response at the cooler temperature
“"Most isolates of human rhinovirus, the common cold virus, replicate more robustly at the cool temperatures found in the nasal cavity (33–35 °C) than at core body temperature (37 °C). [...] These findings demonstrate that in mouse airway cells, rhinovirus replicates preferentially at nasal cavity temperature due, in part, to a less efficient antiviral defense response of infected cells at cool temperature."”
Calculation notes
Foxman et al. supplies the cleanest known mechanism for any cold-exposure- to-cold-illness signal: rhinovirus itself replicates better in a cooler nose, and the innate interferon response is weaker at 33 °C than at 37 °C. This makes Eccles' symptom-onset result biologically plausible without rescuing the folk model. The study is mouse airway cells in vitro, not an epidemiological measurement, and no study has translated the temperature- dependent replication curve into a per-exposure infection probability for a human wearing socks versus going barefoot. The mechanism is real; the epidemiological effect size at normal indoor conditions is not quantified.
Independence note: Yale laboratory study with no authorship, funding, or institutional overlap with the Cardiff Eccles group; treat as methodologically independent mechanistic corroboration. Independent of the CDC and WHO sources.
Source date: 2015-01-20 · Accessed: 2026-04-16
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Rhinovirus-infected mouse airway cells show markedly higher antiviral interferon-response gene expression at 37°C than at 33°C, explaining why the virus replicates more efficiently at cooler nasal-cavity temperatures
“"Most isolates of human rhinovirus, the common cold virus, replicate more robustly at the cool temperatures found in the nasal cavity (33-35 °C) than at core body temperature (37 °C). [...] Mouse airway cells infected with mouse-adapted rhinovirus 1B exhibited a striking enrichment in expression of antiviral defense response genes at 37 °C relative to 33 °C [...] These findings demonstrate that in mouse airway cells, rhinovirus replicates preferentially at nasal cavity temperature due, in part, to a less efficient antiviral defense response of infected cells at cool temperature."”
Calculation notes
Foxman et al. (Yale University) is the mechanistic study the body text and caveats reference as the "kernel of truth" behind the folk belief: rhinovirus replicates preferentially at cooler nasal-cavity temperatures in part because infected airway cells mount a weaker interferon/antiviral response at 33°C than at 37°C. This is an in-vitro mouse-airway-cell study, not a human clinical trial or a measurement of rain-exposure infection rates — it supports biological plausibility for the temperature-dependent effect Eccles (2005) measured in humans, but does not itself quantify any human infection probability. Added as a formal citation because the body text and caveats named this study by author/journal/year without a corresponding sources[] entry.
Independence note: Yale University in-vitro study; institutionally and methodologically independent of the Cardiff Common Cold Centre (Eccles) clinical trial and the Finnish military cohort (Mäkinen et al.) ecological study also cited in this entry.
Source date: 2015-01-20 · Accessed: 2026-07-03
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