Table 1.
Reference and Type of Study | No. of Patients | Main Results |
---|---|---|
Rodriguez et al. [42] Systems-level blood immune-monitoring study |
37 patients | Basophils were depleted during acute disease but increase during recovery. Moreover, levels of basophils were significantly correlated with the titers of IgG antibodies to SARS-CoV-2. |
Mao et al. [43] Observational study |
127 patients admitted at Wuhan No. 1 Hospital | Basophil count was low in 17 (13.39%) patients during the first three days of hospitalization and returned to normal levels shortly after. |
Fátima Conceição-Silva et al. [44] Review discusses the presence of ETs |
ETs produced by neutrophils were associated with severity in SARS-CoV-2 infection favoring thrombosis. ET produced by basophils, which have bacteral killing and antifungal activity, could have a protective role during COVID-19 infection. | |
Ten-Caten et al. [45] A multidimensional analysis |
178,887 Brazilian individuals, of which there were 33,266 positives for SARS-CoV-2 | Lower counts of platelets, basophils, lymphocytes, and eosinophils were observed in COVID-19 cases compared with controls in both males and females. |
Alnor et al. [46] Case–control study |
74 COVID-19-positive and 228 COVID-19-negative patients. | COVID-19 patients presented significant lower values for all white blood cells, including basophil count, in comparison with non-COVID-19 patients. |
Kazancioglu et al. [47] Retrospective case–control study |
120 COVID-19 patients, 100 influenza patients, and 61 healthy controls | Lower basophil count was found both in COVID-19 and influenza patients compared to healthy controls. |
Vitte et al. [48] Observational, prospective, multicentric, case–control study |
26 patients | Low number of basophils were detected in COVID-19 patients as compared with healthy donors. Both CRTH2 (CD294), a receptor for prostaglandin D2, and CD11b expression were decreased at the surface of basophils. SARS-CoV-2 infection was associated with inhibition of T helper 2 polarized immune responses and a decreased chemotaxis of CRTH2+ cells, through reduction of basophils, eosinophils, and CRTH2 itself. |
Chen et al. [49] Retrospective study |
548 patients with COVID-19 |
A difference of basophil levels between admission and end-hospitalization greater than 0.02 × 109/L (HR, 2.73; 95% CI, 1.5–6.47) resulted a risk factor for fatal outcome. |
Laing et al. [50] Observational study |
63 patients | Basophils and dendritic cells are reduced in severe COVID-19. Basophil reduction correlate with elevated interferon-inducible protein-10. |
Qin et al. [51] Observational study |
452 patients admitted at Tongji Hospital | Severe COVID-19 patients had a lower percentage of basophils than non-severe ones (0.1 vs. 0.2%; p = 0.015). |
Sun et al. [52] Mendelian randomization study |
408,112 and 562,132 European subjectsfrom two different GWAS | Negative association between basophil count and basophil percentage of WBC are present in severe and hospitalized COVID-19 disease. |
Motta et al. [53] Histopathological comparative control study |
6 post-mortem covid patients, 10 post-mortem H1N1-infected patients, 10 patients who died for different reasons. | COVID-19 patients samples presented a significantly higher number of mast cells as compared con H1N1 patients and controls. In the context of a neutrophilic endothelitis, mast cells were more frequently localized in the perivascular spaces between the alveolar sacs and terminal bronchioles and in the alveolar septa, close to the alveolar capillaries. |
Bahareh Hafezi et al. [54] cytokine response by mast cells during COVID-19. |
MCs can respond to SARS-CoV-2 and accumulate in the lungs of patients with COVID-19, where they correlate with pulmonary edema, inflammation, and thrombosis. |