Effect of Human Serum Thymic Factor on Immature T Lymphocytes in Acute Leukemia and other Hematologic Malignancies

2015 ◽  
pp. 116-120
Author(s):  
A. O. �avdar ◽  
�. �zger Topuz ◽  
J. Erten ◽  
M. Losio ◽  
M. Erten ◽  
...  
1977 ◽  
Vol 7 (12) ◽  
pp. 836-840 ◽  
Author(s):  
Giulia C.B. Astaldi ◽  
A. Astaldi ◽  
Marjorie Groenewoud ◽  
P. Wijermans ◽  
P.Th.A. Schellekens ◽  
...  

1987 ◽  
Vol 52 (7) ◽  
pp. 1857-1866 ◽  
Author(s):  
Martin Černý ◽  
Evžen Kasafírek ◽  
Jozef Rovenský ◽  
Jan Pekárek

New analogs of the serum thymic factor, (Phe-NH210)-FTS, (Gln1, Phe-NH210)-FTS, and (des Glp1, Phe-NH210)-FTS were synthesized. Their biological activities were evaluated in the recovery assay of T lymphocytes. The activity of (Phe-NH210)-FTS is comparable to the activity of FTS. Nonapeptide (des Glp1, Phe-NH210)-FTS shows the highest activity so far observed. Analog (Gln1, Phe-NH210)-FTS is an inhibitor.


The Lancet ◽  
1977 ◽  
Vol 309 (8011) ◽  
pp. 608 ◽  
Author(s):  
M Pasino ◽  
G.P Tonini ◽  
C Rosanda ◽  
L Massimo

2017 ◽  
Vol 24 (1) ◽  
pp. 61 ◽  
Author(s):  
A. Alghamdi ◽  
A. Lutynski ◽  
M. Minden ◽  
C. Rotstein

Mucormycosis has emerged as an important cause of invasive fungal infection in patients with hematologic malignancies. Gastrointestinal mucormycosis is an unusual presentation of this invasive fungal infection, and it causes considerable morbidity and mortality. Such outcomes are due in part to a nonspecific presentation that results in delays in diagnosis and treatment. Successful treatment of gastrointestinal mucormycosis involves surgical debridement and appropriate antifungal therapy.


2011 ◽  
Vol 4 (4) ◽  
pp. 211
Author(s):  
Serena Meraviglia ◽  
Carmela La Mendola ◽  
Valentina Orlando ◽  
Francesco Scarpa ◽  
Giuseppe Cicero ◽  
...  

The potent anti-tumor activities of γδ T cells, their ability to produce pro-inflammatory cytokines, and their strong cytolytic activity have prompted the development of protocols in which γδ agonists or ex vivo-expanded γδ cells are administered to tumor patients. γδ T cells can be selectively activated by either synthetic phosphoantigens or by drugs that enhance their accumulation into stressed cells as aminobisphosphonates, thus offering new avenues for the development of γδ T cell-based immunotherapies. The recent development of small drugs selectively activating Vγ9Vδ2 T lymphocytes, which upregulate the endogenous phosphoantigens, has enabled the investigators to design the experimental approaches of cancer immunotherapies; several ongoing phase I and II clinical trials are focused on the role of the direct bioactivity of drugs and of adoptive cell therapies involving phosphoantigen- or aminobisphosphonate-activated Vγ9Vδ2 T lymphocytes in humans. In this review, we focus on the recent advances in the activation/expansion of γδ T cells in vitro and in vivo that may represent a promising target for the design of novel and highly innovative immunotherapy in patients with hematologic malignancies.<br />


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