COVID-19-sensitive tumour response: 2-year assessment of the SARS-CoV-2 humoral response in cancer patients in oncology hospital in Poland.

COVID-19-sensitive tumour response: 2-year assessment of the SARS-CoV-2 humoral response in cancer patients in oncology hospital in Poland.

Publication date: Dec 21, 2024

Vaccination has been considered the most crucial defence against viral infections, including SARS-CoV-2. Numerous reports have demonstrated the effectiveness of the above vaccines in oncological patients. It has also been proven that, apart from vaccinations and oncological therapy, the course of the cancer process itself influences the magnitude of the humoral response, especially in people after infection with SARS-CoV-2. The phenomenon we observe seems to confirm the presence of a “natural” defence potential in a cancer patient’s body, in this case, directed against infection with a viral pathogen. A “stronger” antiviral response also explains the asymptomatic course of SARS-CoV-2 infection in some of the above patients. To what extent the SARS-CoV-2 infection weakened the “natural” potential of the anticancer response in these patients remains an open question. This study aimed to answer the question about the impact of the cancer process on the humoral response in oncological patients vaccinated against SARS-CoV-2 infection and in patients after COVID-19. One thousand six hundred and sixty-eight people were observed. Over 2 years, 5,082 SARS-CoV-2 IgG and IgM antibody samples were determined. The concentration of antibodies was assessed in groups of oncological patients: those undergoing anticancer therapy after contracting COVID-19 and those after vaccination against the SARS-CoV-2 infection. The obtained results indicate a naturally more significant humoral response in oncological patients who have not been vaccinated and have not undergone anticancer therapy, such as radiotherapy, chemotherapy, or surgical intervention. The above observation applies to patients with breast, lung, colon, kidney, and testicular cancer, although the response varies significantly depending on the type of cancer.

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Concepts Keywords
Cancer Adult
Kidney Aged
Vaccination Aged, 80 and over
Viral Antibodies, Viral
Antibodies, Viral
Breast cancer
Colon cancer
COVID-19
COVID-19
COVID-19 Vaccines
COVID-19 Vaccines
Female
Humans
Immunity, Humoral
Immunoglobulin G
Immunoglobulin G
Immunoglobulin M
Immunoglobulin M
Lung cancer
Male
Middle Aged
Neoplasms
Poland
SARS-CoV-2
SARS-CoV-2
Vaccination

Semantics

Type Source Name
disease MESH COVID-19
disease MESH cancer
disease MESH viral infections
disease IDO process
disease MESH infection
disease IDO pathogen
pathway REACTOME SARS-CoV-2 Infection
disease IDO intervention
disease MESH testicular cancer
disease MESH Bone Diseases
disease MESH syndrome
drug DRUGBANK L-Phenylalanine
disease MESH asymptomatic infection
disease MESH inflammation
disease MESH long COVID
disease IDO cell
disease MESH lymphomas
disease MESH Hodgkin’s lymphoma
disease MESH multiple myeloma
disease MESH prostate cancer
pathway KEGG Prostate cancer
disease IDO blood
disease MESH complications
disease MESH autoimmune diseases
disease IDO history
drug DRUGBANK Etoperidone
drug DRUGBANK Coenzyme M
drug DRUGBANK Aspartame
drug DRUGBANK Indoleacetic acid
disease IDO entity
disease MESH Polyps
disease MESH Thyroid nodule
drug DRUGBANK Methylergometrine
disease MESH Gastritis
disease MESH Hypothyroidism
disease MESH Ovarian cyst
disease MESH Glioblastoma
disease MESH hyperplasia
disease MESH Diverticulitis
disease MESH Lipoma
disease MESH Sarcoma
disease MESH Nephrolithiasis 1
disease MESH papilloma
disease MESH Fibroma
disease MESH mesothelioma
disease MESH Endometriosis
disease MESH Carcinoid
disease MESH Pancreatic cyst
disease MESH Hernia
disease MESH warts
disease MESH Astrocytoma
disease MESH Prostatitis
disease MESH fibrosis
disease MESH Cervical dysplasia
disease MESH Abscesses
disease MESH neuroma
disease MESH Nevus flammeus
disease MESH Neuralgia
disease MESH Adenomyosis
disease MESH Tinea corporis
disease MESH Rheumatoid arthritis
pathway KEGG Rheumatoid arthritis
disease MESH Herpes simplex
disease MESH COPD
disease MESH Hyperthyroidism
disease MESH Fatty liver
disease MESH Psoriasis
disease MESH Ulcerative colitis
disease MESH Autoimmune thyroiditis
disease MESH Obstructive Pulmonary Disease
disease MESH carcinoma
disease MESH breast cysts
disease MESH breast cancer
pathway KEGG Breast cancer
disease MESH colon cancer
disease MESH kidney cancer
disease MESH breast diseases
disease MESH lung cancer
disease MESH Graves’ disease
drug DRUGBANK Polyethylene glycol
pathway REACTOME Immune System
disease MESH contraindications
disease MESH reinfections
disease MESH herpes zoster
disease IDO immunosuppression
disease MESH obesity
disease MESH hypertension
disease MESH seroconversion
pathway REACTOME Reproduction
drug DRUGBANK Troleandomycin
drug DRUGBANK (S)-Des-Me-Ampa
drug DRUGBANK Guanosine
disease MESH coronavirus infection
disease MESH death
drug DRUGBANK Trestolone

Original Article

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