scholarly journals Immune Cells Have Sex and So Should Journal Articles

Endocrinology ◽  
2012 ◽  
Vol 153 (6) ◽  
pp. 2544-2550 ◽  
Author(s):  
Sabra L. Klein

Males and females have the same immunological cells, proteins, and pathways in place to protect against the development of disease. The kinetics, magnitude, and skewing of the responses mounted against pathogens, allergens, toxins, or self-antigens, however, can differ dramatically between the sexes. Generally, females mount higher innate and adaptive immune responses than males, which can result in faster clearance of pathogens but also contributes to increased susceptibility to inflammatory and autoimmune diseases in females compared with males. Hormonal and genetic factors contribute significantly to sex differences in immune function and disease pathogenesis. In particular, the expression of X-linked genes and microRNA as well as sex steroid hormones signaling through hormone receptors in immune cells can affect responses to immunological stimuli differently in males and females. Despite data illustrating profound differences between the sexes in immune function, sex differences in the pathogenesis of disease are often overlooked in biomedical research. Establishing journal policies that require authors to report the sex of their cells, animals, and subjects will improve our understanding of the pathogenesis of diseases, with the long-term goal of personalizing treatments for immune-mediated diseases differently for males and females in an effort to protect us equally.

2021 ◽  
Vol 22 (16) ◽  
pp. 8768
Author(s):  
Sheng-Dean Luo ◽  
Tai-Jan Chiu ◽  
Wei-Chih Chen ◽  
Ching-Shuen Wang

Otolaryngology (also known as ear, nose, and throat (ENT)) diseases can be significantly affected by the level of sex hormones, which indicates that sex differences affect the manifestation, pathophysiology, and outcomes of these diseases. Recently, increasing evidence has suggested that proinflammatory responses in ENT diseases are linked to the level of sex hormones. The sex hormone receptors are present on a wide variety of immune cells; therefore, it is evident that they play crucial roles in regulating the immune system and hence affect the disease progression of ENT diseases. In this review, we focus on how sex hormones, particularly estrogens, regulate ENT diseases, such as chronic rhinosinusitis, vocal fold polyps, thyroid cancer, Sjögren’s syndrome, and head and neck cancers, from the perspectives of inflammatory responses and specialized proresolving mediator-driven resolution. This paper aims to clarify why considering sex differences in the field of basic and medical research on otolaryngology is a key component to successful therapy for both males and females in the future.


Behaviour ◽  
1992 ◽  
Vol 123 (1-2) ◽  
pp. 38-69 ◽  
Author(s):  
Rachel A. Smolker ◽  
Andrew F. Richards ◽  
Richard C. Connor ◽  
John W. Pepper

AbstractPatterns of association among bottlenose dolphins resident in Shark Bay, Western Australia were analyzed using party membership data. Parties contained an average of 4.8 individuals, but party size and composition were unstable. While these temporary parties often contained both males and females, long term consistent associations generally were between members of the same sex. The highest association coefficients, resulting from very frequent co-occurrence within parties were between males and between mothers and offspring. Males formed subgroups of two or three individuals who consistently associated with each other, and these were stable over periods of at least seven years in some cases. Male subgroups preferentially associated with particular other male subgroups. Females associated most consistently with other females, although not to the same extent as some males. Female associations were better described as a network rather than discrete subgroups. Male-female associations were generally inconsistent and depended in part on female reproductive state. Mothers and their offspring associated very consistently for at least 4 years.


2014 ◽  
Vol 281 (1776) ◽  
pp. 20132123 ◽  
Author(s):  
Tim Connallon ◽  
Andrew G. Clark

Sexual antagonism, whereby mutations are favourable in one sex and disfavourable in the other, is common in natural populations, yet the root causes of sexual antagonism are rarely considered in evolutionary theories of adaptation. Here, we explore the evolutionary consequences of sex-differential selection and genotype-by-sex interactions for adaptation in species with separate sexes. We show that sexual antagonism emerges naturally from sex differences in the direction of selection on phenotypes expressed by both sexes or from sex-by-genotype interactions affecting the expression of such phenotypes. Moreover, modest sex differences in selection or genotype-by-sex effects profoundly influence the long-term evolutionary trajectories of populations with separate sexes, as these conditions trigger the evolution of strong sexual antagonism as a by-product of adaptively driven evolutionary change. The theory demonstrates that sexual antagonism is an inescapable by-product of adaptation in species with separate sexes, whether or not selection favours evolutionary divergence between males and females.


1999 ◽  
Vol 77 (6) ◽  
pp. 885-889 ◽  
Author(s):  
A Courtney DeVries ◽  
C Sue Carter

Prairie voles (Microtus ochrogaster) are monogamous rodents in which both sexes form social preferences for a familiar partner. This species exhibits many of the characteristics of monogamy, including long-term social bonds, mate guarding, and biparental care. Although the behaviors associated with the development of partner preferences are superficially similar in males and females, the present study documents sex differences in the temporal parameters of partner preferences in prairie voles. Following nonsexual cohabitation, female prairie voles formed partner preferences more quickly and these preferences lasted longer than in males. These data indicate that sex differences exist in the development and maintenance of social preferences and may reflect differences in the reproductive strategies of male and female prairie voles.


2019 ◽  
Vol 40 (Supplement_1) ◽  
Author(s):  
A Younis ◽  
S Matetzky ◽  
E Masalha ◽  
F Chernomordik ◽  
Y Afel ◽  
...  

Abstract Background Data are scarce regarding sex differences among patients with myocarditis and peri-myocarditis. Our aim was to define the sex differences in clinical characteristics as well as in-hospital outcomes in a cohort of consecutive patients hospitalized due to myocarditis and peri-myocarditis. Methods and results We analyzed data of 322 consecutive patients between January 2007 and October 2017 who were hospitalized with the diagnosis of myocarditis or peri-myocarditis at our medical center. Eighty-four percent of the patients were males. Both males as well as females had similar rates of chronic medical conditions. However, males were more likely to present with ST elevation (75% vs. 44%. P<0.001) as well as PR depression in ECG compared to women and have higher admission troponin levels (7.6±11 vs. 2.3±4, P<0.001). Women were older (45±17 vs. 36±14, P<0.001) and tended to present with a rather normal ECG. There were no differences in the incidence of in-hospital mortality or the need for escalation therapy between male and female patients. However, males were more likely to have ventricular arrhythmias (7% vs. 0%, P=0.05). no differences in long term mortality were observed among males and females. Variable Male (N=272) Female (N=50) P-value Age 36±14 45±17 <0.001 Cardiology Department 243 (90%) 39 (78%) 0.03 Dyspnea 63 (23%) 22 (44%) 0.002 Pericardial chest pain 94 (35%) 20 (40%) 0.52 Admission SBP (mmhg) 122±16 116±16 0.02 Admission HR (b/min) 82±16 89±21 0.04 Normal ECG 37 (14%) 12 (24%) 0.06 ST elevation 204 (75%) 22 (44%) <0.001 LVEF <50% 215 (80%) 45 (90%) 0.08 LGE 176 (88%) 20 (69%) 0.009 Albumin 4±0.3 3.6±0.4 <0.001 Troponin admission 7.6±11 2.3±4 <0.001 Conclusions Male patients, which constitute the majority of patients. Admitted with myocarditis are younger, with higher troponin levels at admission, are more likely to present with ST elevation, and have a higher rate of ventricular arrythmias when compared to women. However, there are no differences in early as well as long term mortality rates between men and women.


2021 ◽  
Author(s):  
José O. Valdebenito ◽  
Kathryn H. Maher ◽  
Gergely Zachar ◽  
Qin Huang ◽  
Zhengwang Zhang ◽  
...  

Abstract Background: Males and females often exhibit different behaviour, life histories and ecology, and sex differences are typically reflected in their brains. Neuronal protection and maintenance include complex processes led by the microglia that also interact with metabolites such as hormones or immune components. Despite increasing interest in sex-specific brain activation in laboratory animals, the crucial significance of immune function protecting in the brain of wildlife is widely lacking. Here, we study sex-specific expression of immune genes in the brain of a small shorebird, the Kentish plover (Charadrius alexandrinus), that is an emerging model of mating system evolution and speciation. We compare immune gene expression patterns between adult males and adult females in two wild breeding populations in contrasting habitats: a coastal sea-level population and a high-altitude inland population in China.Results: Our analysis yielded 379 genes associated with immune function. We show a significant male-biased immune gene upregulation, which is in line with ecological studies that showed higher survival in males than in females. Immune gene expression in the brain did not differ in upregulation between the coastal and inland populations.Conclusions: We discuss the role of dosage compensation in our findings and their evolutionary significance mediated by sex-specific survival and neuronal deterioration. Similar expression profiles in the coastal and inland populations suggest comparable pathogen pressures between the habitats. We call for further studies on gene expressions of males and females in wild population to understand the implications of immune function for life-histories and demography in natural systems.


Blood ◽  
2008 ◽  
Vol 111 (7) ◽  
pp. 3635-3643 ◽  
Author(s):  
Takeshi Azuma ◽  
Sheng Yao ◽  
Gefeng Zhu ◽  
Andrew S. Flies ◽  
Sarah J. Flies ◽  
...  

Abstract B7-H1 is an immunoglobulin-like immune suppressive molecule broadly detectable on the majority of human and rodent cancers, and its functions have been attributed to delivering an inhibitory signal to its counter-receptor programmed death-1 (PD-1) on T cells. Here we report that B7-H1 on cancer cells receives a signal from PD-1 to rapidly induce resistance against T cell–mediated killing because crippling signaling capacity of B7-H1 but not PD-1 ablates this resistance. Importantly, loss of B7-H1 signaling is accompanied by increased susceptibility to immune-mediated tumoricidal activity. In addition to resistance against T-cell destruction, B7-H1+ cancer cells also become refractory to apoptosis induced by Fas ligation or the protein kinase inhibitor Staurosporine. Our study reveals a new mechanism by which cancer cells use a receptor on immune cells as a ligand to induce resistance to therapy.


Author(s):  
Thea Magrone ◽  
Manrico Magrone ◽  
Matteo Antonio Russo ◽  
Emilio Jirillo

Background: Platelets are cellular fragments derived from bone-marrow megacaryocytes and they are mostly involved in haemostasis and coagulation. However, according to recent data, platelets are able to perform novel immune functions. In fact, they possess a receptorial armamentarium on their membrane for interacting with innate and adaptive immune cells. In addition, platelets also secrete granules which contain cytokines and chemokines for activating and recruiting even distant immune cells. Objectives: The participation of platelets in inflammatory processes will be discussed also in view of their dual role in terms of triggering or resolving inflammation. Involvement of platelets in disease will be illustrated, pointing to their versatile function to either up- or down-regulate pathological mechanisms. Finally, despite the availability of some anti-platelet agents, such as aspirin, dietary manipulation of platelet function is currently investigated. In this regard, special emphasis will be placed on dietary omega-3 polyunsaturated fatty acids (PUFAs) and polyphenol effects on platelets. Conclusion: Platelets play a dual role in inflammatory-immune-mediated diseases either activating or deactivating immune cells. Diet based on substances, such as omega-3 PUFAs and polyphenols, may act as a modulator of platelet function, even if more clinical trials are needed to corroborate such a contention.


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