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Immune System

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VIDEOS

The Incredible Secrets Hidden in Your Immune System | Beck Brachman | TED - YouTube

Overview

An Overview of Our Immune System - YouTube

Immune System, Part 1: Crash Course Anatomy & Physiology #45 - YouTube

Immune System, Part 2: Crash Course Anatomy & Physiology #46 - YouTube

How Does Our Immune System Protect Us?

How Does Our Immune System Protect Us? - YouTube

Dr.SHIVA™: Immune System @CytoSolve® Systems Analysis(12/21) - YouTube

Want to Know your Real Immune System Age? Here You Go!
Bacterial Infections
Elements of the Immune System and Their Roles in Defense - Part 1 (2023 Update)
Elements of the Immune System and Their Roles in Defense - Part 2 (2023 Update)
Immune System Overview (video)
Cells and Tissues of the Immune System
Sensing from within: how the immune system discriminates friend from foe
The Necessity of the Immune System
How the immune system recognize foreign substances
The Immune System: Science Isn't Always Wise
The Social Life of Your Immune System
A Deeper Insight into the Immune System: Why it Matters (video)
Second & Third Line of Defense (Non-Specific)
Little Known Jobs of the Immune System
Biological sex influences peripheral blood immune cells
Defining Trained Immunity and its Role in Health and Disease
Does Your Immune System Listen to Your Thoughts? (video)
How Degenerative Diseases Weaken Your Immune System (video)
Tuning the metabolic drivers of immune cells
"These scientists have figured out how to block the brakes of the immune system."

Cells of the immune response differ from cells of the inflammatory response in 3 ways:

  1. Specificity (adaptive immune system)
  2. "lasting memory" (adaptive immune system)
  3. Antigens trigger the immune response

The colon wall is the largest immune organ in the body. The intestinal mucosa is the battlefield on which friends and foes need to be recognized and properly managed to find the ideal balance between tolerance (a state of health) and immune response (a state of inflammation). Despite it's complexity, mistakes are rarely made, but when they are, we pay a high price. See Intestinal Mucosal Barrier

Several cells play a role in maintaining gut immune homeostasis:

The vagus nerve's regulation of inflammation is involved in immune system activity. During infection or injury, sensory input triggered by inflammation travels through the afferent vagus nerve to the brainstem, from which efferent nerves send signals that terminate in the spleen and other tissues. This assists in communication between immune cells, indicating that the vagus nerve is important for optimal functioning of the immune system.

Diagram of Immune Cells in Lymph Nodes:

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On the left, the dendritic cell arrives in the lymph node and releases:

IL-1 (its job is to introduce fever and activate the inflammatory system;

IL6 - its job is to kick the liver into making acute phase proteins which are part of the innate arm and help with inflammation, it also causes fever by going to the hypothalamus and changing our temperature set point;

IL-12 helps transform naive T cells into TH1 cells;

IL-23 helps activate TH17 cells;

TNF

If the naive T cell is showered by IL-4 it will transform into a TH2 cell provided the naive T cells was primed first by multiple connections to the dendritic cell forming a synapse (see B-Cells), The TH2 cell will release IL-13, IL-10, IL-4 and IL-5.

IL-13 has an interesting behavior. First, it acts on a B cell to perform a class switching and can help it class switch to IgE. It can also act on the innate arm to change the behavior. IL-13 can transform the macrophage into an alternate macrophage called an M2 macropage. (see M1 and M2 Macrophage)

Similarly IL-4 can act on a B-cell to class switch it to IgE. . Both Il-4 and IL-5 help the B-cell proliferate and become differentiated.

IL-5 can help a B-cell class switch to IgA as well as help activate eosinophils and other cells.

IL-10 is interesting, it acts on the innate arm and helps tone down the activity of the innate arm. It reduces the activity of macrophages, it is anti-inflammatory.

On the lower part of the diagram we see how TH1 becomes activated when the naive T cell gets showered with IL-12 after it has has bound in a synapse with the dendritic cell. The TH1 cell releases interferon gamma back to the dendritic cell which is a potent magnifier of macrophages and dendritic cells.

TH2 reduces the activity of the macrophages and dendritic cells, TH1 amplies them.

The IL-4 produced by TH2 can act on TH1 to tame them down. When a pathogen arrives in our body, its possible the immune system would activate both arms (innate and acquired) but one arm will become dominant so either the humoral arm (the B-cell antibody arm) or the cytotoxic T-cell arm. When one arm becomes dominant it releases interleukins to suppress the other arm. We don’t want both arms to be active at the same time with the same potency. When IL-4 suppresses TH1 it suppressed the cytotoxic T-Cell side.

Note that in the activation stage, TH2 is bound to the B-cell through the synapse, then the TH2 cell releases IL-4 and IL-5 to make the B-cell active. The activated B-cell becomes a plasma cell with a very unique nucleus under the microscope, the nucleus looks like a sailor’s wheel. Because it is active producing a lot of antibodies (proteins) it’s genes are open to continuously make antibodies.

In our body the circulating proteins such as albumin, globulins, complement system , haptoglobins, ferritins, are produced by the liver. The liver is the largest contributor of proteins circulating in us. The secondary largest contributor are B-Cells which make antibodies that are circulating in us and antibodies will help clear out pathogens.

If we look at the route shown on the lower part of the diagram where cytotoxic T-cells are produced, the humoral route, the dendritic cell or macrophage presents the antigen to naive T-cells, in the presence of IL-12 which comes from the macrophage or dendritic cell. Then the naive T-cell actually becomes a TH1 cell. The TH1 cell releases interferon gamma to help boost the dendritic cell or macrophage. It would also release IL-2 to activate a cytotoxic T-cell (it does not need a synapse) that is bound to an infected or cancerous cell it will become angry and pump out perforins and granzymes that kill this cell. They are also called “killer T-cells”.

The acquired arm has many interleukins that would affect the innate arm and vice versa.

Articles/Studies

Imprinting of the immune system by the microbiota early in life

Study ties recently discovered immune cell to disease

Ancient gene influences immunity of First Nations Peoples of Oceania

The gut microbiota, its relationship to the immune system, and possibilities of its modulation.

Diverse Roles of Mitochondria in Immune Responses: Novel Insights Into Immuno-Metabolism

The Emerging Role of the Mammalian Glycocalyx in Functional Membrane Organization and Immune System Regulation

Atossa -- The protein queen commanding cell invasion Immune cells are our body's police force, but how can they reach the crime scene fast? Researchers have now discovered a new protein that boosts energy production inside immune cells and thus increases their power to invade. Apart from improving immune responses, the results could revolutionize our understanding of energy regulation in cells throughout the human body.

The immune system is very complicated, but now, it's on a chip

The intestinal neuro-immune axis: crosstalk between neurons, immune cells, and microbes

Immune cells forget (cell) culture shock A recent study shows that certain immune cells can restore their normal functions when introduced back into the body, even after being multiplied in the laboratory to large numbers -- the results pave the way to new cell therapies.

The immune system also helps a healthy body Were you also under the impression that the immune system only kicks in when you get sick? In fact, new research shows the immune system is also busy when you're perfectly healthy. For instance, it helps you convert fat into energy when you're fasting. Until recently, it was believed that the immune system was mostly dormant unless the body was under attack in connection with infections. However, it now turns out that the immune system most likely also plays an important role for perfectly healthy people and can affect the body's production of vital energy sources.Specifically, the immune system causes the liver of the healthy body to produce an energy source called ketone bodies. This takes place by letting the liver burn fat during fasting.

Energy for the brain

"When we're fasting -- that is, we haven't eaten anything for maybe half a day or a full day -- we start drawing on our fat deposits, but not all of our body cells are capable of burning fat. This applies, among other things, to the brain, which instead depends on the production of ketone bodies, which the liver forms by metabolising fats. The ketone bodies thereby energise the body, allowing us to function even if we don't eat anything, explains another lead author of the study," Søren Fisker Schmidt, Assistant Professor at the Department of Biochemistry and Molecular Biology.

Ketone bodies are also the focal point of many popular weight loss diets focusing on cutting carbohydrates from our food, so the body begins burning fat instead. Other research also suggests that the ketone bodies may have a positive impact on, among other things, risk factors for the development of cardiovascular disease.

"We now believe that the immune system affects the production of ketone bodies in fit and healthy individuals and given the beneficial effects of ketone bodies in various common metabolic disorders, this knowledge can hopefully also be applied to understand how the immune system is trying to keep the body in equilibrium when we're sick," Anne Loft explains

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