scholarly journals Molecular evolution of affinity and flexibility in the immune system

2007 ◽  
Vol 104 (21) ◽  
pp. 8821-8826 ◽  
Author(s):  
I. F. Thorpe ◽  
C. L. Brooks
1992 ◽  
Vol 267 (23) ◽  
pp. 16007-16010
Author(s):  
J.D. Marks ◽  
H.R. Hoogenboom ◽  
A.D. Griffiths ◽  
G Winter

2006 ◽  
Vol 22 (12) ◽  
pp. 662-670 ◽  
Author(s):  
P TIFFIN ◽  
D MOELLER

BioEssays ◽  
1997 ◽  
Vol 19 (9) ◽  
pp. 777-786 ◽  
Author(s):  
Austin L. Hughes ◽  
Meredith Yeager

1994 ◽  
Vol 91 (23) ◽  
pp. 10769-10770 ◽  
Author(s):  
S. Bartl ◽  
D. Baltimore ◽  
I. L. Weissman

2021 ◽  
Vol 11 (24) ◽  
pp. 11605
Author(s):  
Angela Quirino ◽  
Nadia Marascio ◽  
Giorgio Settimo Barreca ◽  
Luigia Gallo ◽  
Aida Giancotti ◽  
...  

The purpose of this review is to address some of the latest aspects regarding molecular features, pathogenic mechanisms, and immune system response to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), based on recent publications in this field from March 2020 to May 2021. Interpretation keys for periodic re-emergence of coronavirus infections and other lethal viral pandemics are suggested. Antibody-dependent enhancement (ADE) and other potential mechanisms of immune system deception are put forward. Therefore, vaccine development must take into account ADE and other unwanted side effects of immune-based medical intervention. Features reported in our review will allow both clinicians and basic science researchers to take home ideas to improve their knowledge about SARS-CoV-2.


BMC Genomics ◽  
2008 ◽  
Vol 9 (1) ◽  
pp. 227 ◽  
Author(s):  
Anna Cohuet ◽  
Sujatha Krishnakumar ◽  
Frédéric Simard ◽  
Isabelle Morlais ◽  
Anastasios Koutsos ◽  
...  

2021 ◽  
Author(s):  
Ansgar Bokel ◽  
Michael C. Hutter ◽  
Vlada B. Urlacher

Engineered cytochrome P450 monooxygenase CYP154E1 enables the effective synthesis of the potential antidepressant (2R,6R)-hydroxynorketamine via N-demethylation and regio- and stereoselective hydroxylation of (R)-ketamine.


2014 ◽  
Vol 222 (3) ◽  
pp. 148-153 ◽  
Author(s):  
Sabine Vits ◽  
Manfred Schedlowski

Associative learning processes are one of the major neuropsychological mechanisms steering the placebo response in different physiological systems and end organ functions. Learned placebo effects on immune functions are based on the bidirectional communication between the central nervous system (CNS) and the peripheral immune system. Based on this “hardware,” experimental evidence in animals and humans showed that humoral and cellular immune functions can be affected by behavioral conditioning processes. We will first highlight and summarize data documenting the variety of experimental approaches conditioning protocols employed, affecting different immunological functions by associative learning. Taking a well-established paradigm employing a conditioned taste aversion model in rats with the immunosuppressive drug cyclosporine A (CsA) as an unconditioned stimulus (US) as an example, we will then summarize the efferent and afferent communication pathways as well as central processes activated during a learned immunosuppression. In addition, the potential clinical relevance of learned placebo effects on the outcome of immune-related diseases has been demonstrated in a number of different clinical conditions in rodents. More importantly, the learned immunosuppression is not restricted to experimental animals but can be also induced in humans. These data so far show that (i) behavioral conditioned immunosuppression is not limited to a single event but can be reproduced over time, (ii) immunosuppression cannot be induced by mere expectation, (iii) psychological and biological variables can be identified as predictors for this learned immunosuppression. Together with experimental approaches employing a placebo-controlled dose reduction these data provide a basis for new therapeutic approaches to the treatment of diseases where a suppression of immune functions is required via modulation of nervous system-immune system communication by learned placebo effects.


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