locuiam amândoi pe un nor

ieri am văzut că din nor picura
s-a topit și-am căzut înapoi, jos
nu-i nimic, sigur putem zbura
în plus, și aici e frumos

miroase-a dragoste născandă
în luna lui mai
a floare plăpândă
ce-ți spune să stai

Breast is best: Good bacteria arrive from mum's gut via breast milk

http://www.sciencedaily.com/releases/2013/08/130822091026.htm

Fighting bacteria with new genre of antibodies

http://www.sciencedaily.com/releases/2013/04/130424112314.htm

Early infant growth rate linked to composition of gut microbiota

http://www.sciencedaily.com/releases/2013/05/130509091213.htm

A galaxy within us: Our gut microbiota and how it can be programmed by food

http://www.sciencedaily.com/releases/2013/11/131101125411.htm

An altered gut microbiota can predict diabetes

http://www.sciencedaily.com/releases/2013/06/130603092328.htm

Intestinal Bacteria Linked to White Blood Cell Cancer

IBS and Bloating: When Gut Microbiota Gets out of Balance

Decreased Diversity of Bacteria Microbiome in Gut Associated Colorectal Cancer

Chemotherapy: When Intestinal Bacteria Provide Reinforcement

Type 1 diabetes: Gut microbiota networks may influence autoimmune processes

http://www.sciencedaily.com/releases/2014/03/140312082530.htm

Crohn disease - microbiata direct link

http://www.sciencedaily.com/releases/2014/03/140312132617.htm

Immune system's redesigned role in fighting cancerous tumors

Rsearchers in the Cedars-Sinai Samuel Oschin Comprehensive Cancer Institute eradicated solid tumors in laboratory mice using a novel combination of two targeted agents. These two synergistic therapies stimulate an immune response, ultimately allowing solid tumors to act as their own cancer-fighting vaccine.

The study's findings, published in the journal Cancer Research, are the first to use

these combined agents as an immune stimulator and may have the potential to kill

cancerous cells in solid tumors, including some of the most aggressive cancers that

form in the lung and pancreas. Investigators hope to bring this science to early phase

clinical trials in coming months.

"Instead of administering a cancer vaccine to destroy tumors, we hope to modify the

immune system to allow the patient's own tumor to act as a cancer vaccine," said

Hyung Lae Kim, MD, co-medical director of the Urologic Oncology Program and lead

author of the study. "This approach differs from traditional methods, where the

immune system is stimulated by administering a vaccine. Instead, we administer a combination therapy to allow

immune cells, which are capable of killing tumors, to see tumors that were previously invisible to the immune

system."

When an immune system is working properly, diseased cells are captured and killed. However, cancerous

tumors are formed when the immune system is unable to remove these diseased cells. Using an "mTOR

inhibitor," which regulates cellular metabolism, and a CD4 antibody, which helps to initiate an immune response,

researchers increased the immune system's "memory" and ability to recognize and fight off tumors.

"With our approach, investigators simply combine an mTOR inhibitor and CD4 antibody to create an

immunotherapy treatment, requiring no surgery and a drug with virtually no shelf life," said Robert Figlin, MD,

deputy director of the Samuel Oschin Comprehensive Cancer Institute and the Steven Spielberg Family Chair in

Hematology-Oncology. "This broad implication is in contrast to a more traditional vaccine-based approach, which

requires a specialist to surgically remove tumor samples from a patient's body then create a personalized

vaccine approach for one specific patient."

The combination of a CD4 antibody with an mTOR inhibitor may enhance immune memory and eradicate solid

tumors. Additional research is being done to better understand how the drugs work and develop optimal

strategies for applications in patients.

Yanping Wang, MD, project coordinator in the Kim Laboratory at Cedars-Sinai, and Tim Sparwasser, MD, from

the Institute of Infection Immunology at TWINCORE, were involved in the study.

Citation: Cancer Research. 2014 February: Foxp3+ T cells inhibit antitumor immune memory modulated by

mTOR inhibition.

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Story Source:

The above story is based on materials provided by Cedars-Sinai Medical Center.Note: Materials may be 

edited for content and length.

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Journal Reference:

1. Y. Wang, T. Sparwasser, R. Figlin, H. L. Kim. Foxp3 T cells inhibit antitumor immune memory modulated by mTOR inhibition. Cancer Research, 2014; DOI: 10.1158/0008-5472.CAN-13-2928

Source:
http://www.sciencedaily.com/releases/2014/03/140312103145.htm

green teeth in neonatal syndrome

http://www.nejm.org/doi/full/10.1056/NEJMicm1110461

http://www.nejm.org/image-challenge?ci=02062014

cazuri paraziți

http://info.fujita-hu.ac.jp/~tsutsumi/photo/photo195-4.htm