Immune-Modulators and Thyroid Function in Oncological Patients With Hashimoto S Thyroiditis
Immune-Modulators and Thyroid Function in Oncological Patients With Hashimoto S Thyroiditis
Immune-Modulators and Thyroid Function in Oncological Patients With Hashimoto S Thyroiditis
France.
*
Correspondence:
2
Farmacéutico, Biopharmacie, France. Hector Carvallo, Endocrinologist, Member of S.A.E.M., Prof.
Internal Medicine, Argentina.
3
Former Chief, Dept. Oncology, Htal. Rivadavia, Argentina.
Received: 08 May 2021; Accepted: 10 June 2021
Endocrinologist, Member of S.A.E.M., Prof. Internal Medicine,
4
Argentina.
Citation: Francesco Matozza, Guillermo Artero H, Guillermo Artero, et al. Immune-Modulators and Thyroid Function in Oncological
Patients with Hashimoto´S Thyroiditis. Cancer Sci Res. 2021; 4(2): 1-3.
ABSTRACT
Hashimoto's thyroiditis (HT) is a form of chronic lymphocytic thyoriditis, of autoimmune origin and multiple
physiopathogenic pathways, which may or may not be associated with other autoantibody diseases, both
endocrinological (P.A.S.) and non-endocrinological (M.A.S.). Likewise, HT can coincide -in the same patient- with
very varied oncological pathologies, with which it can interact in a usually negative way. In this article, the benefit
achieved in cancer patients who also had HT is evaluated through the use of immune-modulators.
Keywords
Hashimoto, Oncology, Immune-modulators.
Introduction
Hashimoto's thyroiditis (HT) is the most common cause of
hypothyroidism worldwide (0.3-1.5 cases per 1,000 individuals
per year) [1]. It is 7 times more frequent in the female sex. It is
considered a disease of autoimmune origin, although a large
number of dissimilar factors affect its physiopathogenesis [2,3].
Likewise, an increased incidence of cancer has been observed and
confirmed in patients with autoimmune diseases [4].
Method
Figure 2: Types of tumors in the subjects that were controlled. T3, T4, TSH, TPO and TG antibodies were measured before, during,
and up to 8 months after treatment with immune-modulators. The
immune-modulators were administered orally, sublingually, at a
dose of 4 ml per day.
Results
87 patients (78.5%) treated with Immunomodulators showed an
increase in T3, T4 and a decrease in TSH, TPO and TG antibodies,
two months after starting treatment. 8 (8.16%) patients showed
no changes in thyroid function. 3 patients (3.06%) abandoned
the treatment. Objectively, an increase in white blood cells, red
blood cells, improvement of dry skin, asthenia, depression and
intolerance to cold were observed. Subjectively, we observed
a better quality of life in these patients treated with Immune-
modulators (Figure 6).
Immune-Modulator
The immune-modulator, which was used, is composed of Zinc,
Selenium, Magnesium and Astragalus extract (Astragalus
membranaceus) [5,6]. The constituents of this last compound are:
glycosides, polysaccharides, isoflavone-type flavonoids, sucrose,
phytosterols, such as beta-phytosterol. Astragalus has immune
stimulating properties; it increases immune response, increases the
activity of T lymphocytes and the absolute number of lymphocytes,
stimulates the natural production of interferon and enhances its
activity (Figure 4 and 5). Figure 6: Results.
They stimulate the immune system and improve the quality of life
of these patients. In patients with coexisting Hashimoto's thyroiditis,
immune-modulators show a marked clinical and laboratory improvement,
with a marked reduction in supplementary hormone therapy.
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