Rheumatoid regulatory factor in the blood of rats immunized with autologous lymphocytes, activated <i>in vitro</i> by heterologous lymphocytes

The approaches to prevention of acute and chronic transplant rejection are among the important challenges in clinical transplantology and regenerative medicine. For more than a century, induction of tolerance to natural and artificial transplant antigens has been a desired goal. Recently, anti-lymphocytic antibodies to activated lymphocytes, called regulatory rheumatoid factor (regRF), are shown to be involved in control of autoreactive lymphocytes under normal conditions, thus maintaining natural immune tolerance. A relatively rapid increase in the level of regRF in the blood (3-5 days) after immunization is observed during autotransplantation. Its early rise is also associated with non-reactivity of animals to experimentally induced autoimmune disorders. The aim of our study was to search an opportunity of regRF production in rats by injecting autologous lymphocytes activated in vitro by a heterologous antigen (murine lymphocytes). To achieve this result, a group of rats was immunized intravenously with a mixed culture of autologous and heterologous (murine) lymphocytes (MLC), after 5 days of co-incubation. Another group was immunized with murine lymphocytes only. RegRF in the blood was determined by days 3, 5, 7, 14, 21, 28 and 35 after immunization. It was hypothesized that the intravenous injection of autologous MLC-activated rat lymphocytes and mouse lymphocytes to the rats would cause an early regRF response to autologous lymphocytes, and a later response to heterologous mouse lymphocytes. On average, the regRF titer in rats following immunization with murine lymphocytes did not show significant changes. However, a significant increase in the standard deviation was seen only on day 7, thus indicating to a pronounced individual response of rats to the injection of heterologous murine lymphocytes. Immunization of animals with MLC-activated cells caused a two-phase increase of regRF in blood observed on days 5 and 21. An increase in regRF on day 5 after MLC immunization suggests a response to autologous lymphocytes activated by a heterologous antigen. The obtained results open up a prospect for further research aimed at developing novel techniques for inducing acquired tolerance.

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Publication Details

Journal
Russian Journal of Immunology
Published
2025-09-18
DOI
https://doi.org/10.46235/1028-7221-17142-rrf
Primary Topic
T-cell and B-cell Immunology
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article
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article

Rheumatoid regulatory factor in the blood of rats immunized with autologous lymphocytes, activated in vitro by heterologous lymphocytes

Nadezhda Abisheva, Anastasia V. Kryazhevskikh
Russian Journal of Immunology
T-cell and B-cell Immunology
article

Rheumatoid regulatory factor in the blood of rats immunized with autologous lymphocytes, activated in vitro by heterologous lymphocytes

Nadezhda Abisheva, Anastasia V. Kryazhevskikh
article en

Abstract

The approaches to prevention of acute and chronic transplant rejection are among the important challenges in clinical transplantology and regenerative medicine. For more than a century, induction of tolerance to natural and artificial transplant antigens has been a desired goal. Recently, anti-lymphocytic antibodies to activated lymphocytes, called regulatory rheumatoid factor (regRF), are shown to be involved in control of autoreactive lymphocytes under normal conditions, thus maintaining natural immune tolerance. A relatively rapid increase in the level of regRF in the blood (3-5 days) after immunization is observed during autotransplantation. Its early rise is also associated with non-reactivity of animals to experimentally induced autoimmune disorders. The aim of our study was to search an opportunity of regRF production in rats by injecting autologous lymphocytes activated in vitro by a heterologous antigen (murine lymphocytes). To achieve this result, a group of rats was immunized intravenously with a mixed culture of autologous and heterologous (murine) lymphocytes (MLC), after 5 days of co-incubation. Another group was immunized with murine lymphocytes only. RegRF in the blood was determined by days 3, 5, 7, 14, 21, 28 and 35 after immunization. It was hypothesized that the intravenous injection of autologous MLC-activated rat lymphocytes and mouse lymphocytes to the rats would cause an early regRF response to autologous lymphocytes, and a later response to heterologous mouse lymphocytes. On average, the regRF titer in rats following immunization with murine lymphocytes did not show significant changes. However, a significant increase in the standard deviation was seen only on day 7, thus indicating to a pronounced individual response of rats to the injection of heterologous murine lymphocytes. Immunization of animals with MLC-activated cells caused a two-phase increase of regRF in blood observed on days 5 and 21. An increase in regRF on day 5 after MLC immunization suggests a response to autologous lymphocytes activated by a heterologous antigen. The obtained results open up a prospect for further research aimed at developing novel techniques for inducing acquired tolerance.

Russian Journal of ImmunologyVol. 28(3)
Udmurt Federal Research Center, Ural Branch of the Russian Academy of Sciences (RU), Udmurt State University (RU)
Openalex Percentile: Top 73%
T-cell and B-cell Immunology
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